Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
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TITLE
REDUCING BYPRODUCTION OF MALONATES IN A FERMENTATION
PROCESS
This application claims the benefit of U.S. Provisional Application No.
61/138922, filed December 18, 2008.
FIELD OF THE INVENTION
This invention is in the field of biotechnology. More specifically, this
invention pertains to methods useful for reducing the by-production of organic
acids, and in particular malonates, during fermentation of an organism, based
on expression of a gene encoding malonyl-CoA synthetase.
BACKGROUND OF THE INVENTION
Fermentation is a process to produce one or more products from one
or more substrates through use of a biocatalyst, wherein the biocatalyst can
be a whole microorganism, an isolated enzyme, or any combination thereof.
In a batch fermentation, fermentation begins with a culturing process in
which the medium is inoculated with the desired microbial organism. Growth
or metabolic activity then occurs. The metabolite and biomass compositions
of the system change constantly up to the time the culture is terminated.
Typically, the growth rate of the microbial cells proceeds through a static
lag
phase, to a high-growth log phase (or exponential growth), and finally to a
stationary phase, wherein growth is diminished or halted. Although
production of the microbial product typically occurs during the high-growth
log
phase, this phase of growth cannot continue indefinitely because the medium
becomes depleted of nutrients and enriched with products, if the product is
secreted, and byproducts, as a result of the cultured organisms' growth.
Byproducts may comprise among other things, polysaccharides,
carbohydrates, amino acids, proteins, salts and various organic acids such as
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lactic acid, acetic acid, formic acid, proprionic acid, pyruvate, fumarate,
citrate, isocitrate, glyocylate, succinate, a-ketoglutarate and malonates.
Fermentation is an important technology for biosynthesis of a variety of
microbial products, including amino acids, ethanol, polyunsaturated fatty
acids and antibiotics. The fermentative production and commercialization of
a few chemicals have been reported (W. Crueger and A. Crueger,
Biotechnology: A Textbook of Industrial Microbiology, Sinauer Associates:
Sunderland, MA., pp 124-174 (1990); B. Atkinson and F. Mavituna,
Biochemical Engineering and Biotechnology Handbook, 2nd ed.; Stockton:
New York, pp 243-364 (1991)). Biocatalytic processes, however, frequently
suffer from several well-known limitations which may include: 1) a relatively
small range of products; 2) low yields, titers and productivities; 3)
difficulty
recovering and purifying products from aqueous solutions; and, 4) generation
of unwanted byproducts. Integrating upstream metabolic engineering (i.e.,
product synthesis) with downstream bioprocess engineering (i.e., product
separation and process design) is critical to reap significant value from
industrial fermentation because process limitations increase the cost of
manufacture of the product of interest.
Although various biochemical, physiological and chemical/physical
factors can affect the productivity of a biocatalytic process, important
factors
include the efficiency of the conversion of the substrate to product and the
optimization of energy/carbon flow into the biochemical pathway that results
in the product of interest. In consideration of these factors, a variety of
metabolic engineering techniques have been developed to facilitate up-
regulating desirable biochemical pathways and down-regulating undesirable
biochemical pathways, such as those that compete with the biosynthetic
pathway of interest or those that interfere with production of a particular
end-
product.
The present disclosure concerns the accumulation of malonates as
byproducts during the fermentative synthesis of a product by an organism.
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Specifically, high productivity and minimal waste byproduct are achieved by
engineering the organism to express a heterologous malonyl-CoA synthetase
to enable the reaction: malonate + ATP + CoA malonyl-CoA + AMP +
pyrophosphate ["PPil. Conversion of the byproduct malonate to malonyl-
CoA permits synthesis of fatty acids within the organism, thereby avoiding
accumulation of malonate "byproducts" that can not be further utilized during
the fermentation. This thereby avoids carbon and energy waste within the
organism, reduces the amount of base required to maintain an optimal pH
range during the fermentation process, and reduces the amount of byproduct
organic acids that require neutralization within the fermentation waste steam.
Heterologous malonyl CoA synthetases have been previously
expressed in microbial organisms to enable enhanced production of various
polyketides (U.S. Pat. 6,939,691, U.S. Pat. App. Pub. No. 2003/0073205). As
summarized in Lomb& F., et al. (Biotechnol. Prog., 17(4):612-7 (2001)), the
productivity of polyketide fermentation processes in natural and heterologous
hosts is frequently limited by the in vivo availability of precursors derived
from
a-carboxylated CoA thioesters such as malonyl-CoA and (25)-methylmalonyl-
CoA. Expression of a malonyl-CoA synthetase can alleviate this limitation
and significantly increase polyketide production. Previous disclosures do not
contemplate expression of a heterologous malonyl CoA synthetase to reduce
production of malonates and thereby avoid carbon and energy waste by the
organism.
Applicants have solved the stated problem whereby malonate
"byproducts" accumulate during the fermentation of an organism, leading to
carbon and energy waste, reduced synthesis of the product of interest and
production of waste streams that require neutralization (thereby increasing
the overall cost of manufacture). Novel organisms expressing heterologous
malonyl CoA synthetase proteins are described herein.
SUMMARY OF THE INVENTION
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In a first embodiment, the invention concerns a transgenic organism
useful in fermentation of at least one product, comprising at least one gene
encoding malonyl-CoA synthetase under control of at least one regulatory
sequence; wherein the transgenic organism produces a reduced amount of
malonates as a fermentation byproduct compared with the amount of
malonates produced by the same organism, whether transgenic or not
transgenic, provided that the organism:
a) does not comprise a gene encoding malonyl-CoA synthetase; or,
b) comprises a gene encoding malonyl-CoA synthetase that is not
expressed.
Preferably, the organism organism accumulates oil in an amount of at
least about 25% of its dry cell weight. The organism can be selected from
the group consisting of algae, fungi, euglenoids, yeast, bacteria and
stramenopiles. More preferably, the organism is an oleaginous yeast
selected from the group consisting of Yarrowia, Candida, Rhodotorula,
Rhodosporidium, Cryptococcus, Trichosporon and Lipomyces.
In a second embodiment, the regularoty comprised by the transgenic
organism of invention further comprises a strong promoter.
In a third embodiment, the transgenic organism of the invention
comprising at least one gene encoding malonyl-CoA synthetase can be in
multicopy.
In a fourth embodiment, the transgenic organism the invention
comprises at least one sequence encoding a malonyl-CoA synthetase
polypeptide having an amino acid sequence selected from the group
consisting of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:8, SEQ ID NO:9, SEQ
ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14,
SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID
NO:19, SEQ ID NO:20, SEQ ID NO:21 and SEQ ID NO:22.
In a fifth embodiment, the transgenic organism of the invention
comprises at least one sequence encoding a malonyl-CoA synthetase
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wherein said sequence is selected from the group consisting of SEQ ID NO:1
and SEQ ID NO:3.
In a sixth embodiment, the transgenic organism of the invention
produces a titer of the at least one product is not reduced relative to the
titer
of the at least one product produced by the same organism, whether
transgenic or not transgenic, provided that the organism:
a) does not comprise a gene encoding malonyl-CoA synthetase; or,
b) comprises a gene encoding malonyl-CoA synthetase that is not
expressed.
In a seventh embodiment, the transgenic organism of the invention
further comprises at least one genetic mutation. This at least one genetic
mutation can be a disruption in at least one native peroxisome biogenesis
factor protein.
In an eighth embodiment, the invention comprises a method for
manipulating the content of malonates in a transgenic organism, comprising:
a) providing a transgenic organism useful in fermentation of at least
one product where the transgenic organism comprises at least one
gene encoding a malonyl-CoA synthetase under the control of
suitable regulatory sequences; and,
b) growing the organism to allow expression of the at least one gene
encoding a malonyl-CoA synthetase, such that the transgenic
organism makes a reduced amount of malonates as a fermentation
byproduct compared with the amount of malonates made by the
same organism, whether transgenic or not transgenic, provided that
the organism:
(i) does not comprise a gene encoding malonyl-CoA synthetase;
or,
(ii) comprises a gene encoding malonyl-CoA synthetase that is
not expressed.
Preferably, the at least one gene encoding a malonyl-CoA synthetase
polypeptide has an amino acid sequence selected from the group consisting
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of SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10,
SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID
NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ
ID NO:20, SEQ ID NO:21 and SEQ ID NO:22. Furthermore, the at least one
gene encoding a malonyl-CoA synthetase is selected from the group
consisting of SEQ ID NO:1 and SEQ ID NO:3.
In a ninth embodiment, the transgenic Yarrowia sp. host cell comprises:
a) at least one genetic mutation, wherein the mutation is a disruption in at
least one native peroxisome biogenesis factor protein; and,
b) at least one gene encoding malonyl-CoA synthetase under control of
at least one regulatory sequence; and,
c) genes encoding a functional polyunsaturated fatty acid biosynthetic
pathway.
BRIEF DESCRIPTION OF THE DRAWINGS AND
SEQUENCE LISTINGS
FIG. 1 consists of FIG. 1A, FIG. 1B, FIG. 1C and FIG. 1D, which
together show a comparison of the DNA sequence of the Rhizobium
leguminosarum bv. viciae 3841 malonyl-CoA synthetase gene (GenBank
Accession No. YP 766603; SEQ ID NO:1) and the synthetic gene (SEQ ID
NO:3) codon-optimized for expression in Yarrowia lipolytica.
FIG. 2 provides a plasmid map for pZP2-MCS.
FIG. 3 consists of FIG. 3A and FIG. 3B, which together illustrate the uo-
3/ w-6 fatty acid biosynthetic pathway, and should be viewed together when
considering the description of this pathway.
FIG. 4 diagrams the development of Yarrowia lipolytica strain Y4305.
The invention can be more fully understood from the following detailed
description and the accompanying sequence descriptions, which form a part
of this application.
The following sequences comply with 37 C.F.R. 1.821-1.825
("Requirements for Patent Applications Containing Nucleotide Sequences
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and/or Amino Acid Sequence Disclosures - the Sequence Rules") and are
consistent with World Intellectual Property Organization (WIPO) Standard
ST.25 (1998) and the sequence listing requirements of the EPO and PCT
(Rules 5.2 and 49.5(a-bis), and Section 208 and Annex C of the
Administrative Instructions). The symbols and format used for nucleotide and
amino acid sequence data comply with the rules set forth in 37 C.F.R. 1.822.
SEQ ID NOs:1-22 are ORFs encoding genes or proteins, or plasmids,
as identified in Table 1.
Table 1: Summary Of Nucleic Acid And Protein SEQ ID Numbers
Description and Abbreviation Nucleic acid Protein
SEQ ID NO. SEQ ID NO.
Rhizobium leguminosarum by. viciae 3841 1 2
malonyl-CoA synthetase (GenBank Accession (1515 bp) (504 AA)
No. YP_766603) ("rMCS")
Synthetic malonyl-CoA synthetase derived 3 4
from Rhizobium leguminosarum bv. viciae (1518 bp) (505 AA)
3841 (GenBank Accession No. YP_766603),
codon-optimized for expression in Yarrowia
lipolytica ("MCS")
Rhizobium trifolii malonyl-CoA synthetase -- 5
(GenBank Accession No. AF117694; (504 AA)
GenBank Accession No. AAC83455)
Plasmid pMCS 6 --
(4238 bp)
Plasmid pZP2-MCS 7 --
(9156 bp)
Rhizobium etli CFN 42 (GenBank Accession -- 8
No. YP_468459) (496 AA)
Sinorhizobium medicae WSM419 (GenBank -- 9
Accession No. YP_001313848) (510 AA)
Mesorhizobium sp. BNC1 (GenBank -- 10
Accession No. YP_674146) (506 AA)
Mesorhizobium loti MAFF303099 (GenBank -- 11
Accession No. NP_105559) (504 AA)
Bradyrhizobium sp. BTAi1 (GenBank -- 12
Accession No. YP_001236428) (508 AA)
Rhodopseudomonas palustris BisA53 -- 13
(GenBank Accession No. YP_779412) (504 AA)
Azorhizobium caulinodans ORS 571 -- 14
(GenBank Accession No. YP_001526214) (508 AA)
Rhodopseudomonas palustris BisB5 -- 15
(GenBank Accession No. YP_567622) (503 AA)
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Bradyrhizobium sp. 0RS278 (GenBank -- 16
Accession No. YP_001202443) (508 AA)
Xanthobacter autotrophicus Py2 (GenBank -- 17
Accession No. YP_001415433) (509 AA)
Rhodopseudomonas palustris HaA2 -- 18
(GenBank Accession No. YP_483951) (511 AA)
Oligotropha carboxidovorans 0M5 (GenBank -- 19
Accession No. YP_002210100) (532 AA)
Rhodopseudomonas palustris CGA009 -- 20
(GenBank Accession No. NP_945574) (503 AA)
Bradyrhizobium japonicum USDA 110 -- 21
(GenBank Accession No. NP_767149) (509 AA)
Paracoccus denitrificans PD1222 (GenBank -- 22
Accession No. ZP_00629462) (503 AA)
DETAILED DESCRIPTION OF THE INVENTION
Described herein are generalized methods to avoid accumulation of
malonate "byproducts" that cannot be further utilized during a fermentation,
during production of a product. These methods rely on expression of a
heterologous malonyl-CoA synthetase protein within the host. These
methods have wide-spread applicability because they reduce byproduction of
malonates by a variety of organisms, including algae, fungi, euglenoids,
yeast, bacteria and stramenopiles, during the production of a variety of
products via fermentation. These methods were performed in an oleaginous
yeast, specifically, Yarrowia lipolytica, which had been previously
genetically
engineered to produce polyunsaturated fatty acids ["PUFAs"]. The genetic
mutations relating to engineering production of PUFAs were found to result in
increased byproduction of malonates during the fermentation (malonates
accounted for ¨45% of the total organic acids accumulated). Expression of a
heterologous malonyl-CoA synthetase reversed this effect and resulted in
substantially reduced byproduction of malonates.
In this disclosure, the following abbreviations are used: .
"Open reading frame" is abbreviated as "ORF".
"Polymerase chain reaction" is abbreviated as "PCR".
"American Type Culture Collection" is abbreviated as "ATCC".
"Polyunsaturated fatty acid(s)" is abbreviated as "PUFA(s)".
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"Triacylglycerols" are abbreviated as "TAGS".
"Total fatty acids" are abbreviated as "TFAs".
"Fatty acid methyl esters" are abbreviated as "FAMEs".
"Dry cell weight" is abbreviated as "DCW".
"Co enzyme A" is abbreviated as "CoA".
As used herein, the term "invention" or "present invention" is not meant
to be limiting but applies generally to any of the inventions defined in the
claims or described herein.
The term "malonic acid", also referred to as propanedioic acid
according to International Union of Pure and Applied Chemistry ["IUPAC"]
systematic nomenclature, refers to a dicarboxylic acid having the chemical
structure set forth as CH2(COOH)2. The malonate or propanedioate ion is
derived from malonic acid by loss of two hydrogen ions, (i.e., CH2(C00)22-).
Salts and esters of malonic acid include, but are not limited to, diethyl
malonate [(C21-15)2(C3H204)], dimethyl malonate RCH3)2(C3H204)] and
disodium malonate [Na2(C31-1204)].
As used herein, "malonates" refer to the ionised form of malonic acid,
as well as its esters and salts. All of these are referred to herein
collectively
as "malonates".
As used herein, "malonyl-CoA" [CAS Registry No. 524-14-1] refers to
an acyl thioester that can be formed by the carboxylation of acetyl-CoA to
malonyl-CoA. Alternatively, malonyl-CoA is produced enzymatically from the
substrate malonate, via a malonyl-CoA synthetase.
As used herein, "malonyl-CoA synthetase" [EC 6.2.1.-] catalyzes the
following enzymatic reaction: malonate + ATP + CoA malonyl-
CoA + AMP
+ pyrophosphate ["PPi"]. The enzyme was first purified from malonate-grown
Pseudomonas fluorescens (Kim, Y.S. and S.K. Bang, J. Biol. Chem.,
260:5098-5104 (1985)), although various Rhizobia homologs have since
been isolated from bacteroids within legume nodules (see, for example, Kim,
Y.S. and H.Z. Chae, Biochem. J., 273:511-516 (1991) and Kim, Y.S. and
S.W. Kang, Biochem. J., 297:327-333 (1994)).
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The term "rMCS" refers to a gene (SEQ ID NO:1) encoding a malonyl-
CoA synthetase enzyme (SEQ ID NO:2) from Rhizobium leguminosarum bv.
viciae 3841 (GenBank Accession No. YP 766603). Similarly, the term "MCS"
refers to a synthetic gene encoding malonyl-CoA synthetase derived from
Rhizobium leguminosarum bv. viciae 3841 that is codon-optimized for
expression in Yarrowia lipolytica (i.e., SEQ ID NOs:3 and 4).
The term "Rhizobium" refers to a genus of Gram-negative soil bacteria
(comprising over 30 different species) that fix nitrogen, i.e., diazotrophy.
Rhizobium form an endosymbiotic nitrogen-fixing association with roots of
legumes, such as peas, beans, clover and soy. The bacteria colonize plant
cells within root nodules, convert atmospheric nitrogen to ammonia and then
provide organic nitrogenous compounds such as glutamine or ureides to the
plant. The plant provides the bacteria organic compounds made by
photosynthesis. Based on recent studies, R. trifolii is a later synonym of R.
leguminosarum (M.H. Ram frez-Bahena et al., Int. J. Syst. Evol. Microbiol.,
58:2484-2490 (2008)).
"Fermentation" refers to a process that catalyzes a reaction(s) to
produce product(s) from substrate(s) through use of a biocatalyst(s).
A "biocatalyst" initiates or modifies the rate of a chemical reaction
between substrate(s) and product(s). The biocatalyst can be a whole
microorganism, an isolated enzyme, or any combination thereof. For the
purposes described herein, the biocatalyst will be a whole microorganism,
such as an algae, fungus, euglenoid, yeast, bacteria or stramenopile.
A "fermenter" or "bioreactor" refers to a vessel capable of containing a
fermentation process. The fermenter is a heterogeneous system having two
or more phases, e.g., liquid, gas, solid. Optimal conditions for fermentation
necessitate efficient transfer of mass, heat and momentum from one phase to
the other. A fermenter provides for the following: 1) agitation (for mixing of
cells and medium); 2) aeration, for 02 supply; 3) regulation of factors like
temperature, pH, pressure, aeration, nutrient feeding, liquid level, etc.; 4)
sterilization and maintenance of sterility; and, 5) withdrawal of cells/medium
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(for continuous fermenters). Generally, 20-25% of fermenter volume is left
unfilled with medium as "head space" to allow for splashing, foaming and
aeration. The fermenter design varies greatly depending on the type of
fermentation for which it is used. Modem fermenters are usually integrated
with computers for efficient process monitoring, data acquisition, etc.
The term "broth" or "medium" refers to a liquid solution containing
nutrients for culturing microorganisms, generally comprising water, an energy
source, a carbon source, a nitrogen source and micronutrients. During and/or
at the end of fermentation, the broth may additionally contain the
biocatalyst,
product synthesized by the biocatalyst, metabolic intermediates, byproducts
and other media components such as salts, vitamins, amino acids, cofactors
and antibiotics.
"Product" refers to any biocatalytically-produced primary product of
interest that results from the fermentation. This may be a compound naturally
produced by the biocatalyst or non-native genes may be genetically
engineered into the microorganism for their functional expression during the
fermentation.
In contrast, the term "byproduct" refers to a secondary or incidental
product derived from the conversion by the biocatalyst of substrate(s) to
product(s). Often, it is desirable to selectively remove "byproducts" from the
fermentation system to eliminate feedback inhibition and/or to maximize
biocatalyst activity. Typical fermentation byproducts may include, for
example: polysaccharides, carbohydrates, amino acids, proteins, salts and
various organic acids such as lactic acid, acetic acid, formic acid,
proprionic
acid, pyruvate, fumarate, citrate, isocitrate, glyocylate, succinate, a-
ketoglutarate and malonates.
"Volumetric productivity" refers to the mass of product produced in a
fermenter in a given volume per time, with units of grams/(liter hour)
(abbreviated g/(L hr)). This measure is determined by the specific activity of
the biocatalyst and the concentration of the biocatalyst. It is calculated
from
the titer, run time, and the working volume of the fermenter.
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"Titer" refers to the concentration of product with units of grams/liter
(abbreviated g/L).
The term "conserved domain" or "motif" refers to a set of amino acids
conserved at specific positions along an aligned sequence of evolutionarily
related proteins. While amino acids at other positions can vary between
homologous proteins, amino acids that are highly conserved at specific
positions indicate amino acids that are essential in the structure, the
stability,
or the activity of a protein. Because they are identified by their high degree
of
conservation in aligned sequences of a family of protein homologues, they
can be used as identifiers, or "signatures", to determine if a protein with a
newly determined sequence belongs to a previously identified protein family.
The term "oleaginous" refers to those organisms that tend to store their
energy source in the form of oil (Weete, In: Fungal Lipid Biochemistry, 2nd
Ed., Plenum, 1980). Generally, the cellular oil content of oleaginous
microorganisms follows a sigmoid curve, wherein the concentration of lipid
increases until it reaches a maximum at the late logarithmic or early
stationary growth phase and then gradually decreases during the late
stationary and death phases (Yongmanitchai and Ward, Appl. Environ.
Microbiol., 57:419-25 (1991)). It is common for oleaginous microorganisms to
accumulate in excess of about 25% of their dry cell weight as oil.
The term "oleaginous yeast" refers to those microorganisms classified
as yeasts that can make oil. Examples of oleaginous yeast include, but are
no means limited to, the following genera: Yarrowia, Candida, Rhodotorula,
Rhodosporidium, Cryptococcus, Trichosporon and Lipomyces.
The term "lipids" refer to any fat-soluble (i.e., lipophilic), naturally-
occurring molecule. Lipids are a diverse group of compounds that have many
key biological functions, such as structural components of cell membranes,
energy storage sources and intermediates in signaling pathways. Lipids may
be broadly defined as hydrophobic or amphiphilic small molecules that
originate entirely or in part from either ketoacyl or isoprene groups. The
National Institute of General Medical Sciences (Bethesda, MD) provides a
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general overview of lipids, based on the Lipid Metabolites and Pathways
Strategy (LIPID MAPS) classification system.
The term "oil" refers to a lipid substance that is liquid at 25 C and
usually polyunsaturated. In oleaginous organisms, oil constitutes a major part
of the total lipid. "Oil" is composed primarily of triacylglycerols ["TAGs"]
but
may also contain other neutral lipids, phospholipids and free fatty acids. The
fatty acid composition in the oil and the fatty acid composition of the total
lipid
are generally similar; thus, an increase or decrease in the concentration of
PUFAs in the total lipid will correspond with an increase or decrease in the
concentration of PUFAs in the oil, and vice versa.
The term "triacylglycerols" ["TAGs"] refers to neutral lipids composed of
three fatty acyl residues esterified to a glycerol molecule. TAGs can contain
long chain PUFAs and saturated fatty acids, as well as shorter chain
saturated and unsaturated fatty acids.
The term "fatty acids" refers to long chain aliphatic acids (alkanoic
acids) of varying chain lengths, from about 012 to 022, although both longer
and shorter chain-length acids are known. The predominant chain lengths
are between 016 and 022. The structure of a fatty acid is represented by a
simple notation system of "X:Y", where X is the total number of carbon ["C"]
atoms in the particular fatty acid and Y is the number of double bonds.
Additional details concerning the differentiation between "saturated fatty
acids" versus "unsaturated fatty acids", "monounsaturated fatty acids" versus
"polyunsaturated fatty acids" ["PUFAs"], and "omega-6 fatty acids" rw-6" or
"n-61 versus "omega-3 fatty acids" rw-3" or "n-31 are provided in U.S. Pat.
No. 7,238,482, which is hereby incorporated herein by reference.
Nomenclature used to describe PUFAs herein is given in Table 2. In
the column titled "Shorthand Notation", the omega-reference system is used
to indicate the number of carbons, the number of double bonds and the
position of the double bond closest to the omega carbon, counting from the
omega carbon, which is numbered 1 for this purpose. The remainder of the
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Table summarizes the common names of w-3 and w-6 fatty acids and their
precursors, the abbreviations that are used throughout the specification and
the chemical name of each compound.
Table 2: Nomenclature of Polyunsaturated Fatty Acids And Precursors
Common Name Abbreviation Chemical Name Shorthand
Notation
Myristic -- Tetradecanoic 14:0
Palmitic PaImitate Hexadecanoic 16:0
Palmitoleic -- 9-hexadecenoic 16:1
Stearic -- Octadecanoic 18:0
Oleic cis-9-octadecenoic 18:1
Linoleic LA cis-9, 12-octadecadienoic 18:2 w-6
y-Linolenic GLA cis-6, 9, 12-octadecatrienoic 18:3 w-6
Eicosadienoic EDA cis-11, 14-eicosadienoic 20:2 w-6
Dihomo-y- DGLA cis-8, 11, 14- eicosatrienoic 20:3 w-6
Linolenic
Arachidonic ARA cis-5, 8, 11, 14- 20:4
w-6
eicosatetraenoic
alLinolenic ALA cis-9, 12, 15- 18:3 w-3
octadecatrienoic
Stearidonic STA cis-6, 9, 12, 15- 18:4
w-3
octadecatetraenoic
Eicosatrienoic ETrA cis-11, 14, 17- eicosatrienoic 20:3 w-3
Eicosa- ETA cis-8, 11, 14, 17- 20:4
w-3
tetraenoic eicosatetraenoic
Eicosa- EPA cis-5, 8, 11, 14, 17- 20:5 w-3
pentaenoic eicosapentaenoic
Docosa- cis-7, 10, 13, 16-
DTA 22:4 w-3
tetraenoic docosatetraenoic
Docosa- cis-4, 7, 10, 13, 16-
DPAn-6 22:5 w-6
pentaenoic docosapentaenoic
Docosa- DPA cis-7, 10, 13, 16, 19- 22:5 w-3
pentaenoic docosapentaenoic
Docosa- DHA cis-4, 7, 10, 13, 16, 19- 22:6 w-3
hexaenoic docosahexaenoic
Although the w-3/ w-6 PUFAs listed in Table 2 are the most likely to be
accumulated in the oil fractions of oleaginous yeast using the methods
described herein, this list should not be construed as limiting or as
complete.
The term "PUFA biosynthetic pathway" refers to a metabolic process
that converts oleic acid to w-6 fatty acids such as LA, EDA, GLA, DGLA,
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ARA, DTA and DPAn-6 and w-3 fatty acids such as ALA, STA, ETrA, ETA,
EPA, DPA and DHA. This process is well described in the literature. See
e.g., Intl. App. Pub. No. WO 2006/052870. Briefly, this process involves
elongation of the carbon chain through the addition of carbon atoms and
desaturation of the elongated molecule through the addition of double bonds,
via a series of special elongation and desaturation enzymes termed "PUFA
biosynthetic pathway enzymes" that are present in the endoplasmic reticulum
membrane. More specifically, "PUFA biosynthetic pathway enzymes" refer to
any of the following enzymes (and genes which encode them) associated
with the biosynthesis of a PUFA, including: A4 desaturase, A5 desaturase, A6
desaturase, Al2 desaturase, A15 desaturase, A17 desaturase, A9
desaturase, A8 desaturase, A9 elongase, 014/16 elongase, 016/18 elongase,
018/20 elongase and/or 020/22 elongase.
The term "desaturase" refers to a polypeptide that can desaturate
adjoining carbons in a fatty acid by removing a hydrogen from one of the
adjoining carbons and thereby introducing a double bond between them.
Desaturation produces a fatty acid or precursor of interest. Despite use of
the
omega-reference system throughout the specification to refer to specific fatty
acids, it is more convenient to indicate the activity of a desaturase by
counting from the carboxyl end of the substrate using the delta-system. Of
particular interest herein are: A8 desaturases, A5 desaturases, A17
desaturases, Al2 desaturases, A4 desaturases, A6 desaturases, A15
desaturases and A9 desaturases. In the art, A15 and A17 desaturases are
also occasionally referred to as "omega-3 desaturases", "w-3 desaturases",
and/or "w-3 desaturases", based on their ability to convert w-6 fatty acids
into
their w-3 counterparts (e.g., conversion of LA into ALA and ARA into EPA,
respectively). It may be desirable to empirically determine the specificity of
a
particular fatty acid desaturase by transforming a suitable host with the gene
for the fatty acid desaturase and determining its effect on the fatty acid
profile
of the host.
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The term "elongase" refers to a polypeptide that can elongate a fatty
acid carbon chain to produce an acid 2 carbons longer than the fatty acid
substrate that the elongase acts upon. This process of elongation occurs in a
multi-step mechanism in association with fatty acid synthase, as described in
U.S. Pat. App. Pub. No. 2005/0132442 and Intl. App. Pub. No. WO
2005/047480. Examples of reactions catalyzed by elongase systems are the
conversion of GLA to DGLA, STA to ETA and EPA to DPA. In general, the
substrate selectivity of elongases is somewhat broad but segregated by both
chain length and the degree and type of unsaturation. For example, a 014/16
elongase will utilize a 014 substrate e.g., myristic acid, a 016/18 elongase
will
utilize a 016 substrate e.g., palmitate, a 018/20 elongase will utilize a 018
substrate (e.g., GLA, STA, LA, ALA) and a 020/22 elongase [also referred to as
a A5 elongase] will utilize a 020 substrate (e.g., ARA, EPA). For the purposes
herein, two distinct types of 018/20 elongases can be defined: a A6 elongase
will catalyze conversion of GLA and STA to DGLA and ETA, respectively,
while a A9 elongase is able to catalyze the conversion of LA and ALA to EDA
and ETrA, respectively.
It is important to note that some elongases have broad specificity and
thus a single enzyme may be capable of catalyzing several elongase
reactions. For example a single enzyme may thus act as both a 016/18
elongase and a 018/20 elongase. It may be desirable to empirically determine
the specificity of a fatty acid elongase by transforming a suitable host with
the
gene for the fatty acid elongase and determining its effect on the fatty acid
profile of the host.
The terms "conversion efficiency" and "percent substrate conversion"
refer to the efficiency by which a particular enzyme, such as a desaturase,
can convert substrate to product. The conversion efficiency is measured
according to the following formula: ([product]/[substrate + product])*100,
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where 'product' includes the immediate product and all products in the
pathway derived from it.
The terms "peroxisome biogenesis factor protein", "peroxin" and "Pex
protein" are interchangeable and refer to proteins involved in peroxisome
biogenesis and/or that participate in the process of importing cellular
proteins
by means of ATP hydrolysis through the peroxisomal membrane. The
acronym of a gene that encodes any of these proteins is "Pex gene". A
system for nomenclature of Pex genes is described by Distel et al., J. Cell
Biol., 135:1-3 (1996). At least 32 different Pex genes have been identified so
far in various eukaryotic organisms. Many Pex genes have been isolated
from the analysis of mutants that demonstrated abnormal peroxisomal
functions or structures. Based on a review by Kiel, J. A. K. W., et al.
(Traffic,
7:1291-1303 (2006)), wherein in silico analysis of the genomic sequences of
17 different fungal species was performed, the following Pex proteins were
identified: Pex1p, Pex2p, Pex3p, Pex3Bp, Pex4p, Pex5p, Pex5Bp, Pex5Cp,
Pex5/20p, Pex6p, Pex7p, Pex8p, Pex10p, Pex12p, Pex13p, Pex14p, Pex15p,
Pex16p, Pex17p, Pex14/17p, Pex18p, Pex19p, Pex20p, Pex21p, Pex21Bp,
Pex22p, Pex22p-like and Pex26p. Thus, each of these proteins is referred to
herein as a "Pex protein", a "peroxin" or a "peroxisome biogenesis factor
protein", and is encoded by at least one "Pex gene".
The terms "polynucleotide", "polynucleotide sequence", "nucleic acid
sequence", "nucleic acid fragment" and "isolated nucleic acid fragment" are
used interchangeably herein. These terms encompass nucleotide sequences
and the like. A polynucleotide may be a polymer of RNA or DNA that is
single- or double-stranded, that optionally contains synthetic, non-natural or
altered nucleotide bases. A polynucleotide in the form of a polymer of DNA
may be comprised of one or more segments of cDNA, genomic DNA,
synthetic DNA, or mixtures thereof. Nucleotides (usually found in their
5'-monophosphate form) are referred to by a single letter designation as
follows: "A" for adenylate or deoxyadenylate (for RNA or DNA, respectively),
"C" for cytidylate or deoxycytidylate, "G" for guanylate or deoxyguanylate,
"U"
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for uridylate, "T" for deoxythymidylate, "R" for purines (A or G), "Y" for
pyrimidines (C or T), "K" for G or T, "H" for A or C or T, "l" for inosine,
and "N"
for any nucleotide.
A nucleic acid fragment is "hybridizable" to another nucleic acid
fragment, such as a cDNA, genomic DNA, or RNA molecule, when a single-
stranded form of the nucleic acid fragment can anneal to the other nucleic
acid fragment under the appropriate conditions of temperature and solution
ionic strength. Hybridization and washing conditions are well known and
exemplified in Sambrook, J., Fritsch, E. F. and Maniatis, T. Molecular
Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory: Cold
Spring Harbor, NY (1989),
particularly Chapter 11 and Table 11.1. The conditions of temperature and
ionic strength determine the "stringency" of the hybridization. Stringency
conditions can be adjusted to screen for moderately similar fragments (such
as homologous sequences from distantly related organisms), to highly similar
fragments (such as genes that duplicate functional enzymes from closely
related organisms). Post-hybridization washes determine stringency
conditions. One set of preferred conditions uses a series of washes starting
with 6X SSC, 0.5% SDS at room temperature for 15 min, then repeated with
2X SSC, 0.5% SDS at 45 C for 30 min, and then repeated twice with 0.2X
SSC, 0.5% SDS at 50 C for 30 min. A more preferred set of stringent
conditions uses higher temperatures in which the washes are identical to
those above except for the temperature of the final two 30 min washes in
0.2X SSC, 0.5% SDS was increased to 60 C. Another preferred set of
highly stringent conditions uses two final washes in 0.1X SSC, 0.1% SDS at
65 C. An additional set of stringent conditions include hybridization at 0.1X
SSC, 0.1% SDS, 65 C and washes with 2X SSC, 0.1% SDS followed by
0.1X SSC, 0.1% SDS, for example.
Hybridization requires that the two nucleic acids contain
complementary sequences, although depending on the stringency of the
hybridization, mismatches between bases are possible. The appropriate
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stringency for hybridizing nucleic acids depends on the length of the nucleic
acids and the degree of complementation, variables well known in the art.
The greater the degree of similarity or homology between two nucleotide
sequences, the greater the value of the thermal melting point ["Tm" or "Tm"]
for hybrids of nucleic acids having those sequences. The relative stability,
corresponding to higher Tm, of nucleic acid hybridizations decreases in the
following order: RNA:RNA, DNA:RNA, DNA:DNA. For hybrids of greater
than 100 nucleotides in length, equations for calculating Tm have been
derived (see Sambrook et al., supra, 9.50-9.51). For hybridizations with
shorter nucleic acids, i.e., oligonucleotides, the position of mismatches
becomes more important, and the length of the oligonucleotide determines its
specificity (see Sambrook et al., supra, 11.7-11.8). In one embodiment the
length for a hybridizable nucleic acid is at least about 10 nucleotides.
Preferably a minimum length for a hybridizable nucleic acid is at least about
15 nucleotides; more preferably at least about 20 nucleotides; and most
preferably the length is at least about 30 nucleotides. Furthermore, the
skilled artisan will recognize that the temperature and wash solution salt
concentration may be adjusted as necessary according to factors such as
length of the probe.
A "substantial portion" of an amino acid or nucleotide sequence is that
portion comprising enough of the amino acid sequence of a polypeptide or
the nucleotide sequence of a gene to putatively identify that polypeptide or
gene, either by manual evaluation of the sequence by one skilled in the art,
or
by computer-automated sequence comparison and identification using
algorithms such as the Basic Local Alignment Search Tool ["BLAST"]
(Altschul, S. F., et al., J. Mol. Biol., 215:403-410 (1993)). In general, a
sequence of ten or more contiguous amino acids or thirty or more nucleotides
is necessary in order to putatively identify a polypeptide or nucleic acid
sequence as homologous to a known protein or gene. Moreover, with
respect to nucleotide sequences, gene specific oligonucleotide probes
comprising 20-30 contiguous nucleotides may be used in sequence-
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dependent methods of gene identification (e.g., Southern hybridization) and
isolation, such as, in situ hybridization of microbial colonies or
bacteriophage
plaques. In addition, short oligonucleotides of 12-15 bases may be used as
amplification primers in PCR in order to obtain a particular nucleic acid
fragment comprising the primers. Accordingly, a "substantial portion" of a
nucleotide sequence comprises enough of the sequence to specifically
identify and/or isolate a nucleic acid fragment comprising the sequence. The
skilled artisan, having the benefit of the sequences as reported herein, may
now use all or a substantial portion of the disclosed sequences for purposes
known to those skilled in this art, based on the methodologies described
herein.
The term "complementary" is used to describe the relationship
between nucleotide bases that are capable of hybridizing to one another. For
example, with respect to DNA, adenosine is complementary to thymine and
cytosine is complementary to guanine.
The terms "homology" and "homologous" are used interchangeably.
They refer to nucleic acid fragments wherein changes in one or more
nucleotide bases do not affect the ability of the nucleic acid fragment to
mediate gene expression or produce a certain phenotype. These terms also
refer to modifications of the nucleic acid fragments such as deletion or
insertion of one or more nucleotides that do not substantially alter the
functional properties of the resulting nucleic acid fragment relative to the
initial, unmodified fragment.
Moreover, the skilled artisan recognizes that homologous nucleic acid
sequences are also defined by their ability to hybridize, under moderately
stringent conditions, such as 0.5 X SSC, 0.1`)/0 SDS, 60 C, with the
sequences exemplified herein, or to any portion of the nucleotide sequences
disclosed herein and which are functionally equivalent thereto. Stringency
conditions can be adjusted to screen for moderately similar fragments.
The term "selectively hybridizes" includes reference to hybridization,
under stringent hybridization conditions, of a nucleic acid sequence to a
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specified nucleic acid target sequence to a detectably greater degree (e.g.,
at
least 2-fold over background) than its hybridization to non-target nucleic
acid
sequences and to the substantial exclusion of non-target nucleic acids.
Selectively hybridizing sequences typically have at least about 80% sequence
identity, or 90% sequence identity, up to and including 100% sequence
identity (i.e., fully complementary) with each other.
The term "stringent conditions" or "stringent hybridization conditions"
includes reference to conditions under which a probe will selectively
hybridize
to its target sequence. Stringent conditions are sequence-dependent and will
be different in different circumstances. By controlling the stringency of the
hybridization and/or washing conditions, target sequences can be identified
which are 100% complementary to the probe (homologous probing).
Alternatively, stringency conditions can be adjusted to allow some
mismatching in sequences so that lower degrees of similarity are detected
(heterologous probing). Generally, a probe is less than about 1000
nucleotides in length, optionally less than 500 nucleotides in length.
Typically, stringent conditions will be those in which the salt
concentration is less than about 1.5 M Na ion, typically about 0.01 to 1.0 M
Na ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is
at
least about 30 C for short probes (e.g., 10 to 50 nucleotides) and at least
about 60 C for long probes (e.g., greater than 50 nucleotides). Stringent
conditions may also be achieved with the addition of destabilizing agents
such as formamide. Exemplary low stringency conditions include
hybridization with a buffer solution of 30 to 35% formamide, 1 M NaCI, 1`)/0
SDS (sodium dodecyl sulphate) at 37 C, and a wash in 1X to 2X SSC (20X
SSC = 3.0 M NaCl/0.3 M trisodium citrate) at 50 to 55 C. Exemplary
moderate stringency conditions include hybridization in 40 to 45% formamide,
1 M NaCI, 1% SDS at 37 C, and a wash in 0.5X to 1X SSC at 55 to 60 C.
Exemplary high stringency conditions include hybridization in 50%
formamide, 1 M NaCI, 1% SDS at 37 C, and a wash in 0.1X SSC at 60 to 65
C. An additional set of stringent conditions include hybridization at 0.1X
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SSC, 0.1% SDS, 65 C and washed with 2X SSC, 0.1% SDS followed by
0.1X SSC, 0.1`)/0 SDS, for example.
Specificity is typically the function of post-hybridization washes, the
important factors being the ionic strength and temperature of the final wash
solution. For DNA-DNA hybrids, the thermal melting point ["Tm"] can be
approximated from the equation of Meinkoth et al., Anal. Biochem., 138:267-
284 (1984): Tm = 81.5 C + 16.6 (log M) + 0.41 (%GC) - 0.61 (`)/0 form) -
500/L; where M is the molarity of monovalent cations, %GC is the percentage
of guanosine and cytosine nucleotides in the DNA, (:)/0 form is the percentage
of formamide in the hybridization solution, and L is the length of the hybrid
in
base pairs. The Tm is the temperature (under defined ionic strength and pH)
at which 50% of a complementary target sequence hybridizes to a perfectly
matched probe. Tm is reduced by about 1 C for each 1`)/0 of mismatching;
thus, Tm, hybridization and/or wash conditions can be adjusted to hybridize to
sequences of the desired identity. For example, if sequences with >90%
identity are sought, the Tm can be decreased 10 C. Generally, stringent
conditions are selected to be about 5 C lower than the Tm for the specific
sequence and its complement at a defined ionic strength and pH. However,
severely stringent conditions can utilize a hybridization and/or wash at 1, 2,
3,
or 4 C lower than the Tm; moderately stringent conditions can utilize a
hybridization and/or wash at 6, 7, 8, 9, or 10 C lower than the Tm; and, low
stringency conditions can utilize a hybridization and/or wash at 11, 12, 13,
14,
15, or 20 C lower than the Tm. Using the equation, hybridization and wash
compositions, and desired Tm, those of ordinary skill will understand that
variations in the stringency of hybridization and/or wash solutions are
inherently described. If the desired degree of mismatching results in a Tm of
less than 45 C (aqueous solution) or 32 C (formamide solution), it is
preferred to increase the SSC concentration so that a higher temperature can
be used. An extensive guide to the hybridization of nucleic acids is found in
Tijssen, Laboratory Techniques in Biochemistry and Molecular Biology--
Hybridization with Nucleic Acid Probes, Part I, Chapter 2 "Overview of
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principles of hybridization and the strategy of nucleic acid probe assays",
Elsevier, New York (1993); and Current Protocols in Molecular Biology,
Chapter 2, Ausubel et al., Eds., Greene Publishing and Wiley-Interscience,
New York (1995). Hybridization and/or wash conditions can be applied for at
least 10, 30, 60, 90, 120 or 240 minutes.
The term "percent identity" refers to a relationship between two or
more polypeptide sequences or two or more polynucleotide sequences, as
determined by comparing the sequences. "Percent identity" also means the
degree of sequence relatedness between polypeptide or polynucleotide
sequences, as the case may be, as determined by the percentage of match
between compared sequences. "Percent identity" and "percent similarity" can
be readily calculated by known methods, including but not limited to those
described in: 1) Computational Molecular Biology (Lesk, A. M., Ed.) Oxford
University: NY (1988); 2) Biocomputinq: Informatics and Genome Projects
(Smith, D. W., Ed.) Academic: NY (1993); 3) Computer Analysis of Sequence
Data, Part I (Griffin, A. M., and Griffin, H. G., Eds.) Humania: NJ (1994);
4) Sequence Analysis in Molecular Biology (von Heinje, G., Ed.) Academic
(1987); and, 5) Sequence Analysis Primer (Gribskov, M. and Devereux, J.,
Eds.) Stockton: NY (1991).
Preferred methods to determine percent identity are designed to give
the best match between the sequences tested. Methods to determine
percent identity and percent similarity are codified in publicly available
computer programs. Sequence alignments and percent identity calculations
may be performed using the MegAlignTM program of the LASERGENE
bioinformatics computing suite (DNASTAR Inc., Madison, WI). Multiple
alignment of the sequences is performed using the "Clustal method of
alignment" which encompasses several varieties of the algorithm including
the "Clustal V method of alignment" and the "Clustal W method of alignment"
(described by Higgins and Sharp, CABIOS, 5:151-153 (1989); Higgins, D.G.
et al., Comput. Appl. Biosci., 8:189-191 (1992)) and found in the MegAlignTM
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(version 8Ø2) program of the LASERGENE bioinformatics computing suite
(DNASTAR Inc.). After alignment of the sequences using either Clustal
program, it is possible to obtain a "percent identity" by viewing the
"sequence
distances" table in the program.
For multiple alignments using the Clustal V method of alignment, the
default values correspond to GAP PENALTY=10 and GAP LENGTH
PENALTY=10. Default parameters for pairwise alignments and calculation of
percent identity of protein sequences using the Clustal V method are
KTUPLE=1, GAP PENALTY=3, WINDOW=5 and DIAGONALS SAVED=5.
For nucleic acids these parameters are KTUPLE=2, GAP PENALTY=5,
WINDOW=4 and DIAGONALS SAVED=4. Default parameters for multiple
alignment using the Clustal W method of alignment correspond to GAP
PENALTY=10, GAP LENGTH PENALTY=0.2, Delay Divergent Seqs( /0)=30,
DNA Transition Weight=0.5, Protein Weight Matrix=Gonnet Series, DNA
Weight Matrix=IUB.
The "BLASTN method of alignment" is an algorithm provided by the
National Center for Biotechnology Information ["NCB11 to compare nucleotide
sequences using default parameters, while the "BLASTP method of
alignment" is an algorithm provided by the NCB! to compare protein
sequences using default parameters.
It is well understood by one skilled in the art that many levels of
sequence identity are useful in identifying polypeptides, from other species,
wherein such polypeptides have the same or similar function or activity.
Suitable nucleic acid fragments, i.e., isolated polynucleotides encoding
polypeptides in the methods and host cells described herein, encode
polypeptides that are at least about 70-85% identical, while more preferred
nucleic acid fragments encode amino acid sequences that are at least about
85-95% identical to the amino acid sequences reported herein. Although
preferred ranges are described above, useful examples of percent identities
include any integer percentage from 50% to 100%, such as 51%, 52%, 53%,
54%, 55%, 56%, 57%, 58%, 59%, 60%, 61%, 62%, 63%, 64%, 65%, 66%,
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67%, 68%, 69%, 70%, 71%, 72%, 73%, 74%, 75%, 76%, 77%, 78%, 79%,
80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%,
93%, 94%, 95%, 96%, 97%, 98% or 99%. Also, of interest is any full-length
or partial complement of this isolated nucleotide fragment.
Suitable nucleic acid fragments not only have the above homologies
but typically encode a polypeptide having at least 50 amino acids, preferably
at least 100 amino acids, more preferably at least 150 amino acids, still more
preferably at least 200 amino acids, and most preferably at least 250 amino
acids.
The term "codon degeneracy" refers to the nature in the genetic code
permitting variation of the nucleotide sequence without affecting the amino
acid sequence of an encoded polypeptide. The skilled artisan is well aware
of the "codon-bias" exhibited by a specific host cell in usage of nucleotide
codons to specify a given amino acid. Therefore, when synthesizing a gene
for improved expression in a host cell, it is desirable to design the gene
such
that its frequency of codon usage approaches the frequency of preferred
codon usage of the host cell.
"Synthetic genes" can be assembled from oligonucleotide building
blocks that are chemically synthesized using procedures known to those
skilled in the art. These oligonucleotide building blocks are annealed and
then ligated to form gene segments that are then enzymatically assembled to
construct the entire gene. Accordingly, the genes can be tailored for optimal
gene expression based on optimization of nucleotide sequence to reflect the
codon bias of the host cell. The skilled artisan appreciates the likelihood of
successful gene expression if codon usage is biased towards those codons
favored by the host. Determination of preferred codons can be based on a
survey of genes derived from the host cell, where sequence information is
available. For example, the codon usage profile for Yarrowia lipolytica is
provided in U.S. Pat. 7,125,672.
"Gene" refers to a nucleic acid fragment that expresses a specific
protein, and which may refer to the coding region alone or may include
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regulatory sequences preceding (5' non-coding sequences) and following
(3' non-coding sequences) the coding sequence. "Native gene" refers to a
gene as found in nature with its own regulatory sequences. "Chimeric gene"
refers to any gene that is not a native gene, comprising regulatory and coding
sequences that are not found together in nature. Accordingly, a chimeric
gene may comprise regulatory sequences and coding sequences that are
derived from different sources, or regulatory sequences and coding
sequences derived from the same source, but arranged in a manner different
than that found in nature. "Endogenous gene" refers to a native gene in its
natural location in the genome of an organism. A "foreign" gene refers to a
gene that is introduced into the host organism by gene transfer. Foreign
genes can comprise native genes inserted into a non-native organism, native
genes introduced into a new location within the native host, or chimeric
genes. A "transgene" is a gene that has been introduced into the genome by
a transformation procedure. A "codon-optimized gene" is a gene having its
frequency of codon usage designed to mimic the frequency of preferred
codon usage of the host cell.
"Coding sequence" refers to a DNA sequence which codes for a
specific amino acid sequence. "Suitable regulatory sequences" refer to
nucleotide sequences located upstream (5' non-coding sequences), within, or
downstream (3' non-coding sequences) of a coding sequence, and which
influence the transcription, RNA processing or stability, or translation of
the
associated coding sequence. Regulatory sequences may include promoters,
enhancers, silencers, 5' untranslated leader sequence (e.g., between the
transcription start site and the translation initiation codon), introns,
polyadenylation recognition sequences, RNA processing sites, effector
binding sites and stem-loop structures.
"Promoter" refers to a DNA sequence capable of controlling the
expression of a coding sequence or functional RNA. In general, a coding
sequence is located 3' to a promoter sequence. Promoters may be derived in
their entirety from a native gene, or be composed of different elements
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derived from different promoters found in nature, or even comprise synthetic
DNA segments. It is understood by those skilled in the art that different
promoters may direct the expression of a gene in different tissues or cell
types, or at different stages of development, or in response to different
environmental or physiological conditions. Promoters that cause a gene to be
expressed in most cell types at most times are commonly referred to as
"constitutive promoters". It is further recognized that since in most cases
the
exact boundaries of regulatory sequences have not been completely defined,
DNA fragments of different lengths may have identical promoter activity.
The terms "3' non-coding sequences" and "transcription terminator"
refer to DNA sequences located downstream of a coding sequence. This
includes polyadenylation recognition sequences and other sequences
encoding regulatory signals capable of affecting mRNA processing or gene
expression. The polyadenylation signal is usually characterized by affecting
the addition of polyadenylic acid tracts to the 3' end of the mRNA precursor.
The 3' region can influence the transcription, RNA processing or stability, or
translation of the associated coding sequence.
"RNA transcript" refers to the product resulting from RNA polymerase-
catalyzed transcription of a DNA sequence. When the RNA transcript is a
perfect complementary copy of the DNA sequence, it is referred to as the
primary transcript or it may be a RNA sequence derived from post-
transcriptional processing of the primary transcript and is referred to as the
mature RNA. "Messenger RNA" or "mRNA" refers to the RNA that is without
introns and which can be translated into protein by the cell. "cDNA" refers to
a double-stranded DNA that is complementary to, and derived from, mRNA.
"Sense" RNA refers to RNA transcript that includes the mRNA and so can be
translated into protein by the cell. "Antisense RNA" refers to a RNA
transcript
that is complementary to all or part of a target primary transcript or mRNA
and that blocks the expression of a target gene (U.S. Pat. No. 5,107,065; Intl
App. Pub. No. WO 99/28508).
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The term "operably linked" refers to the association of nucleic acid
sequences on a single nucleic acid fragment so that the function of one is
affected by the other. For example, a promoter is operably linked with a
coding sequence when it is capable of affecting the expression of that coding
sequence. That is, the coding sequence is under the transcriptional control of
the promoter. Coding sequences can be operably linked to regulatory
sequences in sense or antisense orientation.
The term "recombinant" refers to an artificial combination of two
otherwise separated segments of sequence, e.g., by chemical synthesis or by
the manipulation of isolated segments of nucleic acids by genetic engineering
techniques.
The term "expression", as used herein, refers to the transcription and
stable accumulation of sense (mRNA) or antisense RNA derived from nucleic
acid fragments. Expression may also refer to translation of mRNA into a
polypeptide. Thus, the term "expression", as used herein, also refers to the
production of a functional end-product (e.g., an mRNA or a protein [either
precursor or mature]).
"Transformation" refers to the transfer of a nucleic acid molecule into a
host organism, resulting in genetically stable inheritance. The nucleic acid
molecule may be a plasmid that replicates autonomously, for example, or, it
may integrate into the genome of the host organism. Host organisms
containing the transformed nucleic acid fragments are referred to as
"transgenic", "recombinant", "transformed" or "transformant" organisms.
The terms "plasmid" and "vector" refer to an extra chromosomal
element often carrying genes that are not part of the central metabolism of
the cell, and usually in the form of circular double-stranded DNA fragments.
Such elements may be autonomously replicating sequences, genome
integrating sequences, phage or nucleotide sequences, linear or circular, of a
single- or double-stranded DNA or RNA, derived from any source, in which a
number of nucleotide sequences have been joined or recombined into a
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unique construction that is capable of introducing an expression cassette(s)
into a cell.
The term "expression cassette" refers to a fragment of DNA containing
a foreign gene and having elements in addition to the foreign gene that allow
for enhanced expression of that gene in a foreign host. Generally, an
expression cassette will comprise the coding sequence of a selected gene
and regulatory sequences preceding (5' non-coding sequences) and following
(3' non-coding sequences) the coding sequence that are required for
expression of the selected gene product. Thus, an expression cassette is
typically composed of: 1) a promoter sequence; 2) a coding sequence, i.e.,
open reading frame ["ORF"]; and, 3) a 3' untranslated region, i.e., a
terminator that in eukaryotes usually contains a polyadenylation site. The
expression cassette(s) is usually included within a vector, to facilitate
cloning
and transformation. Different expression cassettes can be transformed into
different organisms including bacteria, yeast, plants and mammalian cells, as
long as the correct regulatory sequences are used for each host.
The terms "recombinant construct", "expression construct" and
"construct" are used interchangeably herein. A recombinant construct
comprises an artificial combination of nucleic acid fragments, e.g.,
regulatory
and coding sequences that are not found together in nature. For example, a
recombinant construct may comprise regulatory sequences and coding
sequences that are derived from different sources, or regulatory sequences
and coding sequences derived from the same source, but arranged in a
manner different than that found in nature. Such a construct may be used by
itself or may be used in conjunction with a vector. If a vector is used, then
the
choice of vector is dependent upon the method that will be used to transform
host cells as is well known to those skilled in the art. For example, a
plasmid
vector can be used. The skilled artisan is well aware of the genetic elements
that must be present on the vector in order to successfully transform, select
and propagate host cells comprising any of the isolated nucleic acid
fragments described herein. The skilled artisan will also recognize that
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different independent transformation events will result in different levels
and
patterns of expression (Jones et al., EMBO J., 4:2411-2418 (1985);
De Almeida et al., Mol. Gen. Genetics, 218:78-86 (1989)), and thus that
multiple events must be screened in order to obtain lines displaying the
desired expression level and pattern.
The term "sequence analysis software" refers to any computer
algorithm or software program that is useful for the analysis of nucleotide or
amino acid sequences. "Sequence analysis software" may be commercially
available or independently developed. Typical sequence analysis software
include, but is not limited to: 1) the GCG suite of programs (Wisconsin
Package Version 9.0, Genetics Computer Group (GCG), Madison, WI);
2) BLASTP, BLASTN, BLASTX (Altschul et al., J. Mol. Biol., 215:403-410
(1990)); 3) DNASTAR (DNASTAR, Inc. Madison, WI); 4) Sequencher (Gene
Codes Corporation, Ann Arbor, MI); and, 5) the FASTA program incorporating
the Smith-Waterman algorithm (W. R. Pearson, Comput. Methods Genome
Res., [Proc. Int. Symp.] (1994), Meeting Date 1992, 111-20. Editor(s): Suhai,
Sandor. Plenum: New York, NY). Within this description, whenever sequence
analysis software is used for analysis, the analytical results are based on
the
"default values" of the program referenced, unless otherwise specified. As
used herein "default values" means any set of values or parameters that
originally load with the software when first initialized.
Standard recombinant DNA and molecular cloning techniques used
herein are well known in the art and are described by Sambrook, J., Fritsch,
E. F. and Maniatis, T., Molecular Cloning: A Laboratory Manual, 2nd ed., Cold
Spring Harbor Laboratory: Cold Spring Harbor, NY (1989) (hereinafter
"Maniatis"); by Silhavy, T. J., Bennan, M. L. and Enquist, L. W., Experiments
with Gene Fusions, Cold Spring Harbor Laboratory: Cold Spring Harbor, NY
(1984); and by Ausubel, F. M. et al., Current Protocols in Molecular Biology,
published by Greene Publishing Assoc. and Wiley-Interscience, Hoboken, NJ
(1987).
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Genes encoding malonyl-CoA synthetases are found in a variety of
organisms, such as Rhizobium, Bradyrhizobium, Mesorhizobium,
Azorhizobium, Sinorhizobium, Nitrobacter, Pseudomonas,
Rhodopseudomonas, Oligotropha, Methylobacterium and Xanthobacter.
See, for example, those provided in Example 1, Table 3, corresponding to
SEQ ID NOs:8-22. The primary role of malonyl-CoA synthetase is the
conversion of the substrates malonate and CoA to yield malonyl-CoA, which
can then be used to produce fatty acids.
A number of studies have been performed to characterize malonyl-
CoA synthetases. For example, the active sites and substrate bindings of the
Rhizobium trifolii malonyl-CoA synthetase, determined from NMR
spectroscopy, site-directed mutagenesis, and comparative modeling
methods, reveal details concerning the structure of the folded protein and
provide support that histidine residue number 206 (His206) therein was
important to enzyme functionality, based on its role in generating the
reaction
intermediate malonyl-AMP (Jung, J.W., et al., Protein Sci., 9:1294-1303
(2000)). The enzyme possesses several AMP binding motifs, as highlighted
in FIG. 3A of Jung et al. Similar analysis concerning the malonyl-CoA
synthetase of Bradyrhizobium japonicum USDA 110 was performed by Koo,
H.M. and Y.S. Kim (Arch. Biochem. Biophys., 378(1):167-74 (2000)).
The malonyl-CoA synthetase sequences in Table 3, or portions of
them, may be used to search for malonyl-CoA synthetase homologs in the
same or other species using sequence analysis software. In general, such
computer software matches similar sequences by assigning degrees of
homology to various substitutions, deletions, and other modifications. Use of
software algorithms, such as the BLASTP method of alignment with a low
complexity filter and the following parameters: Expect value = 10, matrix =
Blosum 62 (Altschul, et al., Nucleic Acids Res., 25:3389-3402 (1997)), is well-
known for comparing any malonyl-CoA synthetase protein in Table 3 against
a database of nucleic or protein sequences and thereby identifying similar
known sequences within a preferred organism.
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Use of a software algorithm to comb through databases of known
sequences is particularly suitable for the isolation of homologs having a
relatively low percent identity to publicly available malonyl-CoA synthetase
sequences, such as those described in Table 3. It is predictable that
isolation
would be relatively easier for malonyl-CoA synthetase homologs of at least
about 70%-85% identity to publicly available malonyl-CoA synthetase
sequences. Further, those sequences that are at least about 85%-90%
identical would be particularly suitable for isolation and those sequences
that
are at least about 90%-95% identical would be the most easily isolated.
Some malonyl-CoA synthetase homologs have also been isolated by
the use of motifs unique to malonyl-CoA synthetase enzymes. For example,
it is well known that malonyl-CoA synthetases all possess AMP binding
motifs. This region of "conserved domain" corresponds to a set of amino
acids that are highly conserved at specific positions, which likely represents
a
region of the malonyl-CoA synthetase protein that is essential to the
structure,
stability or activity of the protein. Motifs are identified by their high
degree of
conservation in aligned sequences of a family of protein homologues. As
unique "signatures", they can determine if a protein with a newly determined
sequence belongs to a previously identified protein family. These motifs are
useful as diagnostic tools for the rapid identification of novel malonyl-CoA
synthetase genes.
Alternatively, the publicly available malonyl-CoA synthetase
sequences or their motifs may be hybridization reagents for the identification
of homologs. The basic components of a nucleic acid hybridization test
include a probe, a sample suspected of containing the gene or gene fragment
of interest, and a specific hybridization method. Probes are typically single-
stranded nucleic acid sequences that are complementary to the nucleic acid
sequences to be detected. Probes are hybridizable to the nucleic acid
sequence to be detected. Although probe length can vary from 5 bases to
tens of thousands of bases, typically a probe length of about 15 bases to
about 30 bases is suitable. Only part of the probe molecule need be
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complementary to the nucleic acid sequence to be detected. In addition, the
complementarity between the probe and the target sequence need not be
perfect. Hybridization does occur between imperfectly complementary
molecules with the result that a certain fraction of the bases in the
hybridized
region are not paired with the proper complementary base.
Hybridization methods are well known. Typically the probe and the
sample must be mixed under conditions that permit nucleic acid hybridization.
This involves contacting the probe and sample in the presence of an
inorganic or organic salt under the proper concentration and temperature
conditions. The probe and sample nucleic acids must be in contact for a long
enough time that any possible hybridization between the probe and the
sample nucleic acid occurs. The concentration of probe or target in the
mixture determine the time necessary for hybridization to occur. The higher
the concentration of the probe or target, the shorter the hybridization
incubation time needed. Optionally, a chaotropic agent may be added, such
as guanidinium chloride, guanidinium thiocyanate, sodium thiocyanate,
lithium tetrachloroacetate, sodium perchlorate, rubidium tetrachloroacetate,
potassium iodide or cesium trifluoroacetate. If desired, one can add
formamide to the hybridization mixture, typically 30-50% (v/v) ['by volume].
Various hybridization solutions can be employed. Typically, these
comprise from about 20 to 60% volume, preferably 30%, of a polar organic
solvent. A common hybridization solution employs about 30-50% v/v
formamide, about 0.15 to 1 M sodium chloride, about 0.05 to 0.1 M buffers
(e.g., sodium citrate, Tris-HCI, PIPES or HEPES (pH range about 6-9)), about
0.05 to 0.2% detergent (e.g., sodium dodecylsulfate), or between 0.5-20 mM
EDTA, FICOLL (Pharmacia Inc.) (about 300-500 kdal), polyvinylpyrrolidone
(about 250-500 kdal), and serum albumin. Also included in the typical
hybridization solution are unlabeled carrier nucleic acids from about 0.1 to
mg/mL, fragmented nucleic DNA such as calf thymus or salmon sperm
DNA or yeast RNA, and optionally from about 0.5 to 2% wt/vol ["A/eight by
volume] glycine. Other additives may be included, such as volume exclusion
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agents that include polar water-soluble or swellable agents (e.g.,
polyethylene
glycol), anionic polymers (e.g., polyacrylate or polymethylacrylate) and
anionic saccharidic polymers, such as dextran sulfate.
Nucleic acid hybridization is adaptable to a variety of assay formats.
One of the most suitable is the sandwich assay format. The sandwich assay
is particularly adaptable to hybridization under non-denaturing conditions. A
primary component of a sandwich-type assay is a solid support. The solid
support has adsorbed or covalently coupled to it immobilized nucleic acid
probe that is unlabeled and complementary to one portion of the sequence.
Any of the malonyl-CoA synthetase nucleic acid fragments described
herein or in public literature, or any identified homologs, may be used to
isolate genes encoding homologous proteins from the same or other species.
Isolation of homologous genes using sequence-dependent protocols is well
known in the art. Examples of sequence-dependent protocols include, but
are not limited to: 1) methods of nucleic acid hybridization; 2) methods of
DNA and RNA amplification, as exemplified by various uses of nucleic acid
amplification technologies, such as polymerase chain reaction ["PCR"] (U.S.
Pat. No.4,683,202); ligase chain reaction ["LCR"] (Tabor, S. et al., Proc.
Natl.
Acad. Sci. U.S.A., 82:1074 (1985)); or strand displacement amplification
["SDA"] (Walker, et al., Proc. Natl. Acad. Sci. U.S.A., 89:392 (1992)); and,
3) methods of library construction and screening by complementation.
For example, genes encoding proteins or polypeptides similar to
publicly available malonyl-CoA synthetase genes or their motifs could be
isolated directly by using all or a portion of those publicly available
nucleic
acid fragments as DNA hybridization probes to screen libraries from any
desired organism using well known methods. Specific oligonucleotide probes
based upon the publicly available nucleic acid sequences can be designed
and synthesized by methods known in the art (Maniatis, supra). Moreover,
the entire sequences can be used directly to synthesize DNA probes by
methods known to the skilled artisan, such as random primers DNA labeling,
nick translation or end-labeling techniques, or RNA probes using available
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in vitro transcription systems. In addition, specific primers can be designed
and used to amplify a part or the full length of the publicly available
sequences or their motifs. The resulting amplification products can be
labeled directly during amplification reactions or labeled after amplification
reactions, and used as probes to isolate full-length DNA fragments under
conditions of appropriate stringency.
Typically, in PCR-type amplification techniques, the primers have
different sequences and are not complementary to each other. Depending on
the desired test conditions, the sequences of the primers should be designed
to provide for both efficient and faithful replication of the target nucleic
acid.
Methods of PCR primer design are common and well known (Thein and
Wallace, "The use of oligonucleotides as specific hybridization probes in the
Diagnosis of Genetic Disorders", in Human Genetic Diseases: A Practical
Approach, K. E. Davis Ed., (1986) pp 33-50, IRL: Herndon, VA; Rychlik, W.,
In Methods in Molecular Biology, White, B. A. Ed., (1993) Vol. 15, pp 31-39,
PCR Protocols: Current Methods and Applications. Humania: Totowa, NJ).
Generally two short segments of available malonyl-CoA synthetase
sequences may be used in PCR protocols to amplify longer nucleic acid
fragments encoding homologous genes from DNA or RNA. PCR may also be
performed on a library of cloned nucleic acid fragments wherein the sequence
of one primer is derived from the available nucleic acid fragments or their
motifs. The sequence of the other primer takes advantage of the presence of
the polyadenylic acid tracts to the 3' end of the mRNA precursor encoding
genes.
The second primer sequence may also be based upon sequences
derived from the cloning vector. For example, the skilled artisan can follow
the RACE protocol (Frohman et al., Proc. Natl. Acad. Sci. U.S.A., 85:8998
(1988)) to generate cDNAs by using PCR to amplify copies of the region
between a single point in the transcript and the 3' or 5' end. Primers
oriented
in the 3' and 5' directions can be designed from the available sequences.
Using commercially available 3' RACE or 5' RACE systems (e.g., BRL,
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Gaithersburg, MD), specific 3' or 5' cDNA fragments can be isolated (Ohara
et al., Proc. Natl. Acad. Sci. U.S.A., 86:5673 (1989); Loh et al., Science,
243:217 (1989)).
Based on any of the well-known methods just discussed, it would be
possible to identify and/or isolate malonyl-CoA synthetase gene homologs in
any preferred organism of choice. The activity of any putative malonyl-CoA
synthetase gene can readily be confirmed by standard biochemical assays
(e.g., see Kim, Y.S. and S.K. Bang. Anal Biochem., 170(1):45-9 (1988)).
Acetyl-CoA is the principle building block for de novo biosynthesis of
fatty acids. Although any compound that can effectively be metabolized to
produce acetyl-CoA can serve as a precursor of fatty acids, glucose is often
the primary source of carbon. Via glycolysis, glucose is converted to
pyruvate, which is transported into the mitochondria to be converted by
pyruvate dehydrogenase to acetyl-CoA. Since acetyl-CoA cannot be
transported directly across the mitochondrial membrane into the cytoplasm,
the two carbons from acetyl-CoA condense with oxaloacetate to yield citrate
(catalyzed by citrate synthase). Citrate is transported directly into the
cytoplasm, where it is cleaved by ATP-citrate lyase to regenerate acetyl-CoA
and oxaloacetate. The oxaloacetate reenters the tricarboxylic acid cycle via
conversion to malate.
The synthesis of malonyl-CoA is the first committed step of fatty acid
biosynthesis, which takes place in the cytoplasm. Malonyl-CoA is produced
via carboxylation of acetyl-CoA by acetyl-CoA carboxylase ["ACC"; EC
6.4.1.2]. Fatty acid synthesis is catalyzed by a multi-enzyme fatty acid
synthase complex ["FAS"; EC 2.3.1.85] and occurs by the condensation of
eight two-carbon fragments (acetyl groups from acetyl-CoA) to form a 16-
carbon saturated fatty acid, palmitate. More specifically, FAS catalyzes a
series of 7 reactions, as summarized below (Smith, S., FASEB J.,
8(15):1248-59 (1994)). First, acetyl-CoA and malonyl-CoA are transferred to
the acyl carrier peptide ["ACP"] of FAS. The acetyl group is then transferred
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to the malonyl group, forming 13-ketobutyryl-ACP and releasing 002. Then,
13-ketobutyryl-ACP undergoes reduction (via 13-ketoacyl reductase) and
dehydration (via 13-hydroxyacyl dehydratase) to form a trans-
monounsaturated fatty acyl group. The double bond is reduced by NADPH,
yielding a saturated fatty- acyl group two carbons longer than the initial
one.
The ability of the butyryl-group to condense with a new malonyl group and
repeat the elongation process is then regenerated. When the fatty acyl group
becomes 16 carbons long, a thioesterase activity hydrolyses it, releasing free
palmitate.
Fatty acid synthesis can be summarized by the following equation
(ignoring H+ and water): acetyl-CoA + 7 malonyl-CoA + 14 NADPH ¨>
palmitate + 7 CO2 + 14 NADP+ + 8 CoA.
Further elongation and oxidation of palmitate can occur in either the
mitochondrion or endoplasmic reticulum. Palmitic acid (16:0) and the C2
elongated form stearic acid (18:0) can be unsaturated to their respective
monounsaturated forms, i.e., palmitoleic acid (16:1) and oleic acid (18:1).
This process is catalyzed at the endoplasmic reticulum membrane and
provides fatty acids for phospholipid biosynthesis. Palmitic acid may be
transported back to the mitochondrial matrix or peroxisomal matrix for
oxidation.
Triacylglycerols ["TAGs"], the primary storage unit for fatty acids, are
formed by a series of reactions that involve: 1) esterification of one
molecule
of acyl-CoA to glycerol-3-phosphate via an acyltransferase to produce
lysophosphatidic acid; 2) esterification of a second molecule of acyl-CoA via
an acyltransferase to yield 1,2-diacylglycerol phosphate, commonly identified
as phosphatidic acid; 3) removal of a phosphate by phosphatidic acid
phosphatase to yield 1,2-diacylglycerol ["DAG"]; and, 4) addition of a third
fatty acid by the action of an acyltransferase to form the TAG.
A wide spectrum of fatty acids can be incorporated into TAGs,
including saturated and unsaturated fatty acids and short-chain and long-
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chain fatty acids. Some non-limiting examples of fatty acids that can be
incorporated into TAGs by acyltransferases include: capric (10:0), lauric
(12:0), myristic (14:0), palmitic (16:0), palmitoleic (16:1), stearic (18:0),
oleic
(18:1), vaccenic (18:1), linoleic (18:2), eleostearic (18:3), y¨linolenic
(18:3), a-
linolenic (18:3), stearidonic (18:4), arachidic (20:0), eicosadienoic (20:2),
dihomo-y¨linolenic (20:3), eicosatrienoic (20:3), arachidonic (20:4),
eicosatetraenoic (20:4), eicosapentaenoic (20:5), behenic (22:0),
docosapentaenoic (22:5), docosahexaenoic (22:6), lignoceric (24:0), nervonic
(24:1), cerotic (26:0) and montanic (28:0) fatty acids.
Described herein are methods for manipulating the content of
malonates in a transgenic organism, wherein said malonates comprise the
ionised form of malonic acid, as well as its esters and salts. The methods
comprise:
a) providing a transgenic organism useful in fermentation of at least one
product where the transgenic organism comprises at least one gene
encoding a malonyl-CoA synthetase under the control of suitable
regulatory sequences; and,
b) growing the organism to allow expression of the at least one gene
encoding a malonyl-CoA synthetase, such that the transgenic
organism makes a reduced amount of malonates as a fermentation
byproduct compared with the amount of malonates made by the same
organism, whether transgenic or not transgenic, provided that the
organism:
(i) does not comprise a gene encoding malonyl-CoA
synthetase; or,
(ii) comprises a gene encoding malonyl-CoA synthetase that is
not expressed.
In some embodiments, the at least one gene encoding a malonyl-CoA
synthetase is encoded by an amino acid sequence selected from the group
consisting of: SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:8, SEQ ID NO:9,
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SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID
NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ
ID NO:19, SEQ ID NO:20, SEQ ID NO:21 and SEQ ID NO:22. The malonyl-
CoA synthetase of SEQ ID NO:2 may be encoded by the nucleotide
sequence set forth as SEQ ID NO:1 or SEQ ID NO:3, for example.
Perferably, the at least one sequence encoding the malonyl-CoA
synthetase is under the control of at least one strong promoter, and one of
skill in the art will appreciate that expression of the gene may also be
increased by expression in multicopy.
Also described herein are transgenic organisms comprising at least
one malonyl-CoA synthetase protein, produced by the methods described
above. More specifically, the specification describes a transgenic organism
useful in fermentation of at least one product, comprising at least one gene
encoding malonyl-CoA synthetase under control of at least one regulatory
sequence; wherein the transgenic organism produces a reduced amount of
malonates as a fermentation byproduct compared with the amount of
malonates produced by the same organism, whether transgenic or not
transgenic, provided that the organism:
a) does not comprise a gene encoding malonyl-CoA synthetase; or,
b) comprises a gene encoding malonyl-CoA synthetase that is not
expressed.
The transgenic organism is preferably selected from the group
consisting of algae, fungi, euglenoids, yeast, bacteria and stramenopiles.
More preferred are those organisms classified as oleaginous, such that they
accumulate at least about 25% of their dry cell weight as oil. For example,
preferred oleaginous yeasts include those from the genera Yarrowia,
Candida, Rhodotorula, Rhodosporidium, Cryptococcus, Trichosporon and
Lipomyces.
The "at least one product" refers to any biocatalytically-produced
primary product(s) of interest which results from the fermentation. The
product may be a compound that is naturally produced by the organism or
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non-native genes may be genetically engineered into the organism for their
functional expression in the fermentation, thereby resulting in a product that
is
not naturally produced by the organism. Notably, the expression of the
heterologous malonyl-CoA synthetase will not have a substantial negative
impact on the volumetric productivity or the final titer of the at least one
product (when compared to the productivity in the same organism, whether
transgenic or not transgenic, provided that the organism (i) does not comprise
a gene encoding malonyl-CoA synthetase; or, (ii) comprises a gene encoding
malonyl-CoA synthetase that is not expressed).
In some embodiments, the transgenic organisms comprising at least
one malonyl-CoA synthetase further comprises at least one genetic mutation.
For example, Applicants observed that disruption in at least one native
peroxisome biogenesis factor protein ["PEX"] in strains of Yarrowia lipolytica
advantageously led to increased production of polyunsaturated fatty acids
["PUFAs"] in the total lipid fraction and in the oil fraction, concurrent with
increased production of byproduct malonates. Construction of several Y.
lipolytica strains comprising PEX disruptions are described in U.S. Pat. App.
No. 12/244950 [E.I. du Pont de Nemours & Co. Inc. Attorney Docket No.
CL3847]; preferred disruptions are within any of the following Pex genes:
YlPex1p (GenBank Accession No. CAG82178), YlPex2p (GenBank
Accession No. CAG77647), YlPex3p (GenBank Accession No. CAG78565),
YlPex3Bp (GenBank Accession No. CAG83356), YlPex4p (GenBank
Accession No. CAG79130), YlPex5p (GenBank Accession No. CAG78803),
YlPex6p (GenBank Accession No. CAG82306), YlPex7p (GenBank
Accession No. CAG78389), YlPex8p (GenBank Accession No. CAG80447),
YlPex12p (GenBank Accession No. CAG81532), YlPex13p (GenBank
Accession No. CAG81789), YlPex14p (GenBank Accession No. CAG79323),
YlPex16p (GenBank Accession No. CAG79622), YlPex17p (GenBank
Accession No. CAG84025), YlPex19p (GenBank Accession No. AAK84827),
YlPex2Op (GenBank Accession No. CAG79226), YlPex22p (GenBank
Accession No. CAG77876) and YlPex26p (GenBank Accession No.
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NC 006072, antisense translation of nucleotides 117230-118387). As
described in the Examples, the increased by-production of malonates in these
Pex-disrupted strains of Yarrowia was substantially reduced by expression of
a heterologous malonyl-CoA synthetase, without negatively affecting the
PUFA productivity.
Thus, in one preferred embodiment of the present invention, a
transgenic Yarrowia sp. host cell is described, the host cell comprising:
a) at least one genetic mutation, wherein the mutation is a disruption in at
least one native peroxisome biogenesis factor protein; and,
b) at least one gene encoding malonyl-CoA synthetase under control of
at least one regulatory sequence; and,
c) genes encoding a functional polyunsaturated fatty acid biosynthetic
pathway.
One of skill in the art will be capable of identifying other genetic
mutations within the transgenic organism that result in production of
unacceptable amounts of malonates during fermentation of the at least one
product. Expression of at least one malonyl-CoA synthetase gene under the
control of at least one regulatory sequence will result in a transgenic
organism that produces a reduced amount of malonates as a fermentation
byproduct compared with the amount of malonates produced by the same
organism, whether transgenic or not transgenic, provided that the organism (i)
does not comprise a gene encoding malonyl-CoA synthetase; or, (ii)
comprises a gene encoding malonyl-CoA synthetase that is not expressed.
It is necessary to create and introduce a recombinant construct
comprising an open reading frame ["ORF"] encoding malonyl-CoA synthetase
into the organism useful in a fermentation. One of skill in the art is aware
of
standard resource materials that describe: 1) specific conditions and
procedures for construction, manipulation and isolation of macromolecules,
such as DNA molecules, plasmids, etc.; 2) generation of recombinant DNA
fragments and recombinant expression constructs; and 3) screening and
isolating of clones. See Sambrook et al., Molecular Cloning: A Laboratory
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Manual, 2nd ed., Cold Spring Harbor Laboratory: Cold Spring Harbor, NY
(1989); Maliga et al., Methods in Plant Molecular Biology, Cold Spring Harbor,
NY (1995); Birren et al., Genome Analysis: Detecting Genes, v. 1, Cold
Spring Harbor, NY (1998); Birren et al., Genome Analysis: Analyzing DNA, v.
2, Cold Spring Harbor: NY (1998); Plant Molecular Biology: A Laboratory
Manual, Clark, ed. Springer: NY (1997).
In general, the choice of sequences included in the construct depends
on the desired expression products, the nature of the host cell and the
proposed means of separating transformed cells versus non-transformed
cells. The skilled artisan is aware of the genetic elements that must be
present on the plasmid vector to successfully transform, select and propagate
host cells containing the chimeric gene. Typically, however, the vector or
cassette contains sequences directing transcription and translation of the
relevant gene(s), a selectable marker and sequences allowing autonomous
replication or chromosomal integration. Suitable vectors comprise a region 5'
of the gene that controls transcriptional initiation, i.e., a promoter, and a
region 3' of the DNA fragment that controls transcriptional termination, i.e.,
a
terminator. It is most preferred when both control regions are derived from
genes from the transformed host cell.
Initiation control regions or promoters useful for driving expression of
heterologous genes or portions of them in the desired host cell are numerous
and well known. These control regions may comprise a promoter, enhancer,
silencer, intron sequences, 3' UTR and/or 5' UTR regions, and protein and/or
RNA stabilizing elements. Such elements may vary in their strength and
specificity. Virtually any promoter, i.e., native, synthetic, or chimeric,
capable
of directing expression of these genes in the selected host cell is suitable.
Expression in a host cell can occur in an induced or constitutive fashion.
Induced expression occurs by inducing the activity of a regulatable promoter
operably linked to the malonyl-CoA synthetase gene of interest. Constitutive
expression occurs by the use of a constitutive promoter operably linked to the
gene of interest.
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When the host cell is, e.g., yeast, transcriptional and translational
regions functional in yeast cells are provided, particularly from the host
species. See Intl. App. Pub. No. WO 2006/052870 for preferred
transcriptional initiation regulatory regions for use in Yarrowia lipolytica.
Any
number of regulatory sequences may be used, depending on whether
constitutive or induced transcription is desired, the efficiency of the
promoter
in expressing the ORF of interest, the ease of construction, etc.
3' non-coding sequences encoding transcription termination signals,
i.e., a "termination region", must be provided in a recombinant construct and
may be from the 3' region of the gene from which the initiation region was
obtained or from a different gene. A large number of termination regions are
known and function satisfactorily in a variety of hosts when utilized in both
the
same and different genera and species from which they were derived. The
termination region is selected more for convenience rather than for any
particular property. Termination regions may also be derived from various
genes native to the preferred hosts.
Particularly useful termination regions for use in yeast are derived from
a yeast gene, particularly Saccharomyces, Schizosaccharomyces, Candida,
Yarrowia or Kluyveromyces. The 3'-regions of mammalian genes encoding y-
interferon and a-2 interferon are also known to function in yeast. The 3'-
region can also be synthetic, as one of skill in the art can utilize available
information to design and synthesize a 3'-region sequence that functions as a
transcription terminator. A termination region may be unnecessary, but is
highly preferred.
The vector may comprise a selectable and/or scorable marker, in
addition to the regulatory elements described above. Preferably, the marker
gene is an antibiotic resistance gene such that treating cells with the
antibiotic
results in growth inhibition, or death, of untransformed cells and uninhibited
growth of transformed cells. For selection of yeast transformants, any marker
that functions in yeast is useful with resistance to kanamycin, hygromycin and
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the amino glycoside G418 and the ability to grow on media lacking uracil,
lysine, histine or leucine being particularly useful.
Merely inserting a gene into a cloning vector does not ensure its
expression at the desired rate, concentration, amount, etc. In response to the
need for a high expression rate, many specialized expression vectors have
been created by manipulating a number of different genetic elements that
control transcription, RNA stability, translation, protein stability and
location,
oxygen limitation, and secretion from the host cell. Some of the manipulated
features include: the nature of the relevant transcriptional promoter and
terminator sequences, the number of copies of the cloned gene and whether
the gene is plasmid-borne or integrated into the genome of the host cell, the
final cellular location of the synthesized foreign protein, the efficiency of
translation and correct folding of the protein in the host organism, the
intrinsic
stability of the mRNA and protein of the cloned gene within the host cell
and the codon usage within the cloned gene, such that its frequency
approaches the frequency of preferred codon usage of the host cell. Each of
these may be used in the methods and host cells described herein to further
optimize expression of malonyl-CoA synthetase genes.
After a recombinant construct is created comprising at least one
chimeric gene comprising a promoter, a malonyl-CoA synthetase ORF and a
terminator, it is placed in a plasmid vector capable of autonomous replication
in the host cell or is directly integrated into the genome of the host cell.
Integration of expression cassettes can occur randomly within the host
genome or can be targeted through the use of constructs containing regions
of homology with the host genome sufficient to target recombination with the
host locus. Where constructs are targeted to an endogenous locus, all or
some of the transcriptional and translational regulatory regions can be
provided by the endogenous locus.
When two or more genes are expressed from separate replicating
vectors, each vector may have a different means of selection and should lack
homology to the other construct(s) to maintain stable expression and prevent
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reassortment of elements among constructs. Judicious choice of regulatory
regions, selection means and method of propagation of the introduced
construct(s) can be experimentally determined so that all introduced genes
are expressed at the necessary levels to provide for synthesis of the desired
products.
Constructs comprising the gene of interest may be introduced into a
host cell by any standard technique. These techniques include
transformation, e.g., lithium acetate transformation (Methods in Enzymology,
194:186-187 (1991)), protoplast fusion, biolistic impact, electroporation,
microinjection, vacuum filtration or any other method that introduces the gene
of interest into the host cell.
For convenience, a host cell that has been manipulated by any method
to take up a DNA sequence, for example, in an expression cassette, is
referred to herein as "transformed" or "recombinant". The transformed host
will have at least one copy of the expression construct and may have two or
more, depending upon whether the gene is integrated into the genome,
amplified, or is present on an extrachromosomal element having multiple
copy numbers.
The transformed host cell can be identified by selection for a marker
contained on the introduced construct. Alternatively, a separate marker
construct may be co-transformed with the desired construct, as many
transformation techniques introduce many DNA molecules into host cells.
Typically, transformed hosts are selected for their ability to grow on
selective media, which may incorporate an antibiotic or lack a factor
necessary for growth of the untransformed host, such as a nutrient or growth
factor. An introduced marker gene may confer antibiotic resistance, or
encode an essential growth factor or enzyme, thereby permitting growth on
selective media when expressed in the transformed host. Selection of a
transformed host can also occur when the expressed marker protein can be
detected, either directly or indirectly. The marker protein may be expressed
alone or as a fusion to another protein. Cells expressing the marker protein
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or tag can be selected, for example, visually, or by techniques such as
fluorescence-activated cell sorting or panning using antibodies.
Regardless of the selected host or expression construct, multiple
transformants must be screened to obtain a strain or line displaying the
desired expression level, regulation and pattern, as different independent
transformation events result in different levels and patterns of expression
(Jones et al., EMBO J., 4:2411-2418 (1985); De Almeida et al., Mol. Gen.
Genetics, 218:78-86 (1989)). Such screening may be accomplished by
Southern analysis of DNA blots (Southern, J. Mol. Biol., 98:503 (1975)),
Northern analysis of mRNA expression (Kroczek, J. Chromatogr. Biomed.
Appl., 618(1-2):133-145 (1993)), Western and/or Elisa analyses of protein
expression, phenotypic analysis or iron chromatography analyses of the
fermentation broth to detect any changes in the organic acid levels.
A variety of eukaryotic organisms are suitable to serve as a transgenic
organism comprising a heterologous malonyl-CoA synthetase, as described
in the methods of the present disclosure. Various fungi, algae, oomycetes,
yeasts, stramenopiles, bacteria and/or euglenoids that can be grown in a
fermenter may be useful hosts.
In some cases, oleaginous organisms are preferred. Oleaginous
organisms are naturally capable of oil synthesis and accumulation, commonly
accumulating in excess of about 25% of their dry cell weight as oil. Various
algae, moss, fungi, yeast, stramenopiles and plants are naturally classified
as
oleaginous. In alternate embodiments, a non-oleaginous organism can be
genetically modified to become oleaginous, e.g., yeast such as
Saccharomyces cerevisiae.
More preferred oleaginous microbes include those algal, stramenopile
and fungal organisms that naturally produce w-3/ w-6 PUFAs. For example,
ARA, EPA and/or DHA is produced via Cyclotella sp., Nitzschia sp., Pythium,
Thraustochytrium sp., Schizochytrium sp. and Mortierella. The method of
transformation of M. alpina is described by Mackenzie et al. (Appl. Environ.
Microbiol., 66:4655 (2000)). Similarly, methods for transformation of
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Thraustochytriales microorganisms (e.g., Thraustochytrium, Schizochytrium)
are disclosed in U.S. Pat. No. 7,001,772.
More preferred are oleaginous yeasts, including those that naturally
produce and those genetically engineered to produce w-3/ w-6 PUFAs (infra).
Genera typically identified as oleaginous yeast include, but are not limited
to:
Yarrowia, Candida, Rhodotorula, Rhodosporidium, Cryptococcus,
Trichosporon and Lipomyces. More specifically, illustrative oil-synthesizing
yeasts include: Rhodosporidium toruloides, Lipomyces starkeyii, L. lipoferus,
Candida revkaufi, C. pulcherrima, C. tropicalis, C. utilis, Trichosporon
pullans,
T. cutaneum, Rhodotorula glutinus, R. graminis and Yarrowia lipolytica
(formerly classified as Candida lipolytica).
The most preferred oleaginous yeast is Yarrowia lipolytica; and most
preferred are Y. lipolytica strains designated as ATCC #76982, ATCC
#20362, ATCC #8862, ATCC #18944 and/or LGAM S(7)1 (Papanikolaou S.,
and Aggelis G., Bioresour. Technol., 82(1):43-9 (2002)).
Specific teachings relating to transformation of Yarrowia lipolytica
include U.S. Pat. No. 4,880,741 and U.S. Pat. No. 5,071,764 and Chen, D. C.
et al. (Appl. Microbiol. Biotechnol., 48(2):232-235 (1997)), while suitable
selection techniques are described in U.S. Pat. No. 7,238,482, U.S. Pat. No.
7,259,255 and Intl App. Pub. No. WO 2006/052870.
The preferred method of expressing genes in Yarrowia lipolytica is by
integration of linear DNA into the genome of the host. Integration into
multiple locations within the genome can be particularly useful when high
level expression of genes is desired, such as in the Ura3 locus (GenBank
Accession No. AJ306421), the Leu2 gene locus (GenBank Accession No.
AF260230), the Lys5 gene locus (GenBank Accession No. M34929), the
Aco2 gene locus (GenBank Accession No. AJ001300), the Pox3 gene locus
(Pox3: GenBank Accession No. XP _503244 or Aco3: GenBank Accession
No. AJ001301), the Al2 desaturase gene locus (U.S. Pat. No. 7,214,491),
the Lipl gene locus (GenBank Accession No. Z50020), the Lip2 gene locus
(GenBank Accession No. AJ012632), the SCP2 gene locus (GenBank
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Accession No. AJ431362), the Pex3 gene locus (GenBank Accession No.
CAG78565), the Pex16 gene locus (GenBank Accession No. CAG79622)
and/or the Pex10 gene locus (GenBank Accession No. CAG81606).
Preferred selection methods for use in Yarrowia lipolytica include
resistance to kanamycin, hygromycin and the amino glycoside G418 and the
ability to grow on media lacking uracil, leucine, lysine, tryptophan or
histidine.
5-fluoroorotic acid [5-fluorouracil-6-carboxylic acid monohydrate or "5-FOX]
may also be used for selection of yeast Ura- mutants. This compound is toxic
to yeast cells that possess a functioning URA3 gene encoding orotidine 5'-
monophosphate decarboxylase [OMP decarboxylase]; thus, based on this
toxicity, 5-FOA is especially useful for the selection and identification of
Ura-
mutant yeast strains (Bartel, P.L. and Fields, S., Yeast 2-Hybrid System,
Oxford University: New York, v. 7, pp 109-147, 1997; see also Intl App. Pub.
No. WO 2006/052870 for 5-FOA use in Yarrowia).
An alternate preferred selection method for use in Yarrowia relies on a
dominant, non-antibiotic marker for Yarrowia lipolytica based on sulfonylurea
(chlorimuron ethyl; E. I. duPont de Nemours & Co., Inc., Wilmington, DE)
resistance. More specifically, the marker gene is a native acetohydroxyacid
synthase ("AHAS" or acetolactate synthase; E.G. 4.1.3.18) that has a single
amino acid change, i.e., W497L, that confers sulfonyl urea herbicide
resistance (Intl App. Pub. No. WO 2006/052870). AHAS is the first common
enzyme in the pathway for the biosynthesis of branched-chain amino acids,
i.e., valine, leucine, isoleucine, and it is the target of the sulfonylurea
and
imidazolinone herbicides.
The transgenic organism is grown under conditions that optimize
production of the at least one product, while controlling the production of
malonates. This will reduce carbon and energy waste within the organism as
well as the amount of byproduct organic acids that require neutralization
during fermentation while maintaining an optimal pH range within the
fermentation waste steam. Optimally, fermentation of the organism
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comprising the heterologous malyonyl-CoA synthetase will reduce the total
cost of manufacture of the at least one product.
In general, media conditions may be optimized by modifying the type
and amount of carbon source, the type and amount of nitrogen source, the
carbon-to-nitrogen ratio, the amount of different mineral ions, the oxygen
level, growth temperature, pH, length of the biomass production phase, length
of the oil accumulation phase and the time and method of cell harvest. For
example, the oleaginous yeast of interest, such as Yarrowia lipolytica, is
generally grown in a complex medium such as yeast extract-peptone-
dextrose broth ["YPD"], a defined minimal media, or a defined minimal media
that lacks a component necessary for growth and forces selection of the
desired expression cassettes (e.g., Yeast Nitrogen Base (DIFCO
Laboratories, Detroit, MI)).
Fermentation media for the methods and transgenic organisms
described herein must contain a suitable carbon source such as taught in
U.S. Pat. No. 7,238,482. Suitable sources of carbon encompass a wide
variety of sources, with sugars such as glucose, fructose, glycerol and/or
fatty
acids being preferred. Most preferred is glucose and/or fatty acids containing
between 10-22 carbons.
Nitrogen may be supplied from an inorganic (e.g., (NH4)2SO4) or
organic (e.g., urea or glutamate) source. In addition to appropriate carbon
and nitrogen sources, the fermentation media must also contain suitable
minerals, salts, cofactors, buffers, vitamins and other components known to
those skilled in the art suitable for the growth of the organism and the
promotion of the enzymatic pathways that enable production of the at least
one product.
It is contemplated that a variety of fermentation process designs (e.g.,
batch, fed-batch or continuous) may be applied for production of the at least
one product. A batch fermentation process is a closed system wherein the
media composition is fixed at the beginning of the process and not subject to
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further additions beyond those required for maintenance of pH and oxygen
level during the process. Thus, at the beginning of the culturing process the
media is inoculated with the desired organism and growth or metabolic
activity occurs without adding additional sources (i.e., carbon and nitrogen
sources) to the medium. In batch processes, the metabolite and biomass
compositions of the system change constantly up to the time the culture is
terminated. In a typical batch process, cells proceed through a static lag
phase to a high-growth log phase and finally to a stationary phase, wherein
the growth rate is diminished or halted. Left untreated, cells in the
stationary
phase will eventually die.
A variation of the standard batch process is the fed-batch process,
wherein the carbon source is continually added to the fermenter over the
course of the fermentation process. A fed-batch process is also suitable
herein. Fed-batch processes are useful when catabolite repression is apt to
inhibit the metabolism of the cells or where it is desirable to have limited
amounts of carbon source in the media at any one time. Measurement of the
carbon source concentration in fed-batch systems is difficult and therefore
may be estimated on the basis of the changes of measurable factors such as
pH, dissolved oxygen and the partial pressure of waste gases (e.g., 002).
Batch and fed-batch culturing methods are common and well known in the art
and examples may be found in Thomas D. Brock in Biotechnology: A
Textbook of Industrial Microbiology, 2nd ed., (1989) Sinauer Associates:
Sunderland, MA; or Deshpande, Mukund V., Appl. Biochem. Biotechnol.,
36:227 (1992).
Alternatively, a continuous fermentation process occurs when a
defined media is continuously added to a bioreactor while an equal amount of
culture volume is removed simultaneously for product recovery. Continuous
cultures generally maintain the cells in the log phase of growth at a constant
cell density. Continuous or semi-continuous culture methods permit the
modulation of one factor or any number of factors that affect cell growth or
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end product concentration. For example, one approach may limit the carbon
source and allow all other parameters to moderate metabolism. In other
systems, a number of factors affecting growth may be altered continuously
while the cell concentration, measured by media turbidity, is kept constant.
Continuous systems strive to maintain steady state growth and thus the cell
growth rate must be balanced against cell loss due to media being drawn off
the culture. Methods of modulating nutrients and growth factors for
continuous culture processes, as well as techniques for maximizing the rate
of product formation, are well known in the art of industrial microbiology and
a
variety of methods are detailed by Brock, supra.
DESCRIPTION OF PREFERRED EMBODIMENTS
The metabolic process wherein oleic acid (18:1) is converted to w-31
w-6 fatty acids involves elongation of the carbon chain through the addition
of
carbon atoms and desaturation of the molecule through the addition of double
bonds. This requires a series of special elongation and desaturation
enzymes present in the endoplasmic reticulum membrane. However, as
seen in FIG. 3 and as described below, there are often multiple alternate
pathways for production of a specific w-31 w-6 fatty acid.
Specifically, FIG. 3 depicts the pathways described below. All
pathways require the initial conversion of oleic acid to linoleic acid ["LA"],
the
first of the w-6 fatty acids, by a Al2 desaturase. Then, using the "A6
desaturase/A6 elongase pathway" and LA as substrate, long-chain w-6 fatty
acids are formed as follows: 1) LA is converted to y-linolenic acid ["GLA"] by
a
A6 desaturase; 2) GLA is converted to dihomoy-y-linolenic acid ["DGLA"] by a
C18/20 elongase; 3) DGLA is converted to arachidonic acid ["ARA"] by a A5
desaturase; 4) ARA is converted to docosatetraenoic acid ["DTA"] by a C20/22
elongase; and, 5) DTA is converted to docosapentaenoic acid ["DPAn-61 by
a A4 desaturase.
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Alternatively, the "A6 desaturase/A6 elongase pathway" can use a-
linolenic acid ["ALA"] as substrate to produce long-chain w-3 fatty acids as
follows: 1) LA is converted to ALA, the first of the w-3 fatty acids, by a A15
desaturase; 2) ALA is converted to stearidonic acid ["STA"] by a A6
desaturase; 3) STA is converted to eicosatetraenoic acid ["ETA"] by a 018/20
elongase; 4) ETA is converted to eicosapentaenoic acid ["EPA"] by a A5
desaturase; 5) EPA is converted to docosapentaenoic acid ["DPA"] by a 020/22
elongase; and, 6) DPA is converted to docosahexaenoic acid ["DHA"] by a A4
desaturase. Optionally, w-6 fatty acids may be converted to w-3 fatty acids.
For example, ETA and EPA are produced from DGLA and ARA, respectively,
by A17 desaturase activity.
Alternate pathways for the biosynthesis of w-3/ w-6 fatty acids utilize
A9 elongase and A8 desaturase, that is, the "A9 elongase/ A8 desaturase
pathway". More specifically, LA and ALA may be converted to EDA and
ETrA, respectively, by a A9 elongase. A A8 desaturase then converts EDA to
DGLA and/or ETrA to ETA. Downstream PUFAs are subsequently formed as
described above.
The transgenic organism herein preferably possesses the ability to
produce PUFAs, either naturally or via techniques of genetic engineering.
Although many microorganisms can synthesize PUFAs (including w-3/ w-6
fatty acids) in the ordinary course of cellular metabolism, some of whom could
be commercially cultured, few to none of these organisms produce oils having
a desired oil content and composition for use in pharmaceuticals, dietary
substitutes, medical foods, nutritional supplements, other food products,
industrial oleochemicals or other end-use applications. Thus, there is
increasing emphasis on the ability to engineer microorganisms for production
of "designer" lipids and oils, wherein the fatty acid content and composition
are carefully specified by genetic engineering. On this basis, it is expected
that the host likely comprises heterologous genes encoding a functional
PUFA biosynthetic pathway but not necessarily.
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If the host organism does not natively produce the desired PUFAs or
possess the desired lipid profile, one skilled in the art is familiar with the
considerations and techniques necessary to introduce one or more
expression cassettes encoding appropriate enzymes for PUFA biosynthesis
into the host organism of choice. Numerous teachings are provided in the
literature to one of skill for so introducing such expression cassettes into
various host organisms. Some references using the host organism Yarrowia
lipolytica are provided as follows: U.S. Pat. No. 7,238,482, U.S. Pat. No.
7,465,564, U.S. Pat. No. 7,550,286, U.S. Pat. No. 7,588,931, U.S. Pat. Appl.
Pub. No. 2006-0115881-A1 and U.S. Pat. Appl. Pub. No. 2009-0093543-A1.
This list is not exhaustive and should not be construed as limiting.
Briefly, a variety of w-3/ w-6 PUFA products can be produced prior to
their transfer to TAGs, depending on the fatty acid substrate and the
particular genes of the w-3/ w-6 fatty acid biosynthetic pathway that are
present in or transformed into the host cell. As such, production of the
desired fatty acid product can occur directly or indirectly. Direct production
occurs when the fatty acid substrate is converted directly into the desired
fatty
acid product without any intermediate steps or pathway intermediates.
Indirect production occurs when multiple genes encoding the PUFA
biosynthetic pathway may be used in combination such that a series of
reactions occur to produce a desired PUFA. Specifically, it may be desirable
to transform an oleaginous yeast with an expression cassette comprising a
Al2 desaturase, A6 desaturase, a 018/20 elongase, a A5 desaturase and a
A17 desaturase for the overproduction of EPA. See U.S. Pat. No. 7,238,482
and Inn App. Pub. No. WO 2006/052870. As is well known to one skilled in
the art, various other combinations of genes encoding enzymes of the PUFA
biosynthetic pathway may be useful to express in an oleaginous organism
(see FIG. 3). The particular genes included within a particular expression
cassette depend on the host organism, its PUFA profile and/or
desaturase/elongase profile, the availability of substrate and the desired end
product(s).
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A number of candidate genes having the desired desaturase and/or
elongase activities can be identified according to publicly available
literature,
such as GenBank, the patent literature, and experimental analysis of
organisms having the ability to produce PUFAs. Useful desaturase and
elongase sequences may be derived from any source, e.g., isolated from a
natural source such as from bacteria, algae, fungi, oomycete, yeast, plants,
animals, etc., produced via a semi-synthetic route or synthesized de novo.
Following the identification of these candidate genes, considerations for
choosing a specific polypeptide having desaturase or elongase activity
include: 1) the substrate specificity of the polypeptide; 2) whether the
polypeptide or a component thereof is a rate-limiting enzyme; 3) whether the
desaturase or elongase is essential for synthesis of a desired PUFA; 4) co-
factors required by the polypeptide; 5) whether the polypeptide is modified
after its production, such as by a kinase or a prenyltransferase; and/or, 6)
whether the polypeptide is physically within an appropriate cellular location
following its production.
The expressed polypeptide preferably has parameters compatible with
the biochemical environment of its location in the host cell. See U.S. Pat.
No.
7,238,482. It may also be useful to consider the conversion efficiency of each
particular desaturase and/or elongase. More specifically, since each enzyme
rarely functions with 100`)/0 efficiency to convert substrate to product, the
final
lipid profile of un-purified oils produced in a host cell is typically a
mixture of
various PUFAs consisting of the desired w-3/ w-6 fatty acid, as well as
various upstream intermediary PUFAs. Thus, the conversion efficiency of
each enzyme is also a variable to consider when optimizing biosynthesis of a
desired fatty acid.
Typically, accumulation of significant amounts of PUFAs and TAGs in
oleaginous yeast cells requires a two-stage process, since the metabolic
state must be "balanced" between growth and synthesis/storage of fats (see,
U.S. Pat. No. 7,238,482). In this approach, the first stage of the
fermentation
is dedicated to the generation and accumulation of cell mass and is
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characterized by rapid cell growth and cell division. In the second stage of
the fermentation, it is preferable to establish conditions of nitrogen
deprivation
in the culture to promote high levels of lipid accumulation. Often, the
carbon/nitrogen ratio is greater than about 40, preferably greater than about
50, and more preferably greater than about 60. The effect of this nitrogen
deprivation is to reduce the effective concentration of AMP in the cells,
thereby reducing the activity of the NAD-dependent isocitrate dehydrogenase
of mitochondria. When this occurs, citric acid will accumulate, thus forming
abundant pools of acetyl-CoA in the cytoplasm and priming fatty acid
synthesis. Thus, this phase is characterized by the cessation of cell division
followed by the synthesis of fatty acids and accumulation of oil.
Preferred growth media for the methods and host cells described
herein are common commercially prepared media, such as Yeast Nitrogen
Base (DIFCO Laboratories, Detroit, MI). Other defined or synthetic growth
media may also be used and the appropriate medium for growth of the
transgenic organism is well known in microbiology or fermentation science. A
suitable pH range for the fermentation is typically between about pH 4.0 to
pH 8.0, wherein pH 5.5 to pH 7.5 is preferred as the range for the initial
growth conditions. The fermentation may be conducted under aerobic or
anaerobic conditions, wherein microaerobic conditions are preferred.
Particular attention is given to several metal ions, such as Fe+2, Cu+2,
Mn+2, Co+2, Zn+2 and Mg+2, that promote synthesis of lipids and PUFAs
(Nakahara, T. et al., Ind. Appl. Single Cell Oils, D. J. Kyle and R. Colin,
eds.
pp 61-97(1992).
EXAMPLES
The present invention is further described in the following Examples,
which illustrate reductions to practice of the invention but do not completely
define all of its possible variations.
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GENERAL METHODS
Standard recombinant DNA and molecular cloning techniques used in
the Examples are well known in the art and are described by: 1) Sambrook,
J., Fritsch, E. F. and Maniatis, T., Molecular Cloning: A Laboratory Manual;
Cold Spring Harbor Laboratory: Cold Spring Harbor, NY (1989) (Maniatis);
2) T. J. Silhavy, M. L. Bennan, and L. W. Enquist, Experiments with Gene
Fusions; Cold Spring Harbor Laboratory: Cold Spring Harbor, NY (1984); and,
3) Ausubel, F. M. et al., Current Protocols in Molecular Biology, published by
Greene Publishing Assoc. and Wiley-Interscience, Hoboken, NJ (1987).
Materials and methods suitable for the maintenance and growth of
microbial cultures are well known in the art. Techniques suitable for use in
the following examples may be found as set out in Manual of Methods for
General Bacteriology (Phillipp Gerhardt, R. G. E. Murray, Ralph N. Costilow,
Eugene W. Nester, Willis A. Wood, Noel R. Krieg and G. Briggs Phillips, Eds),
American Society for Microbiology: Washington, D.C. (1994)); or by Thomas
D. Brock in Biotechnology: A Textbook of Industrial Microbiology, 2nd ed.,
Sinauer Associates: Sunderland, MA (1989). All reagents, restriction
enzymes and materials used for the growth and maintenance of microbial
cells were obtained from Aldrich Chemicals (Milwaukee, WI), DIFCO
Laboratories (Detroit, MI), New England Biolabs, Inc. (Beverly, MA),
GIBCO/BRL (Gaithersburg, MD), or Sigma Chemical Company (St. Louis,
MO), unless otherwise specified. E. coli strains were typically grown at 37 C
on Luria Bertani (LB) plates.
General molecular cloning was performed according to standard
methods (Sambrook et al., supra). DNA sequence was generated on an ABI
Automatic sequencer using dye terminator technology (U.S. Pat. No.
5,366,860; EP 272,007) using a combination of vector and insert-specific
primers. Sequence editing was performed in Sequencher (Gene Codes
Corporation, Ann Arbor, MI). All sequences represent coverage at least two
times in both directions. Unless otherwise indicated herein comparisons of
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genetic sequences were accomplished using DNASTAR software (DNASTAR
Inc., Madison, WI). The meaning of abbreviations is as follows: "sec" means
second(s), "min" means minute(s), "h" means hour(s), "d" means day(s), "pL"
means microliter(s), "mL" means milliliter(s), "L" means liter(s), "pM" means
micromolar, "mM" means millimolar, "M" means molar, "mmol" means
millimole(s), "pmole" mean micromole(s), "g" means gram(s), "pg" means
microgram(s), "ng" means nanogram(s), "U" means unit(s), "bp" means base
pair(s) and "kB" means kilobase(s).
Nomenclature For Expression Cassettes:
The structure of an expression cassette is represented by a simple
notation system of "X::Y::Z", wherein X describes the promoter fragment, Y
describes the gene fragment, and Z describes the terminator fragment, which
are all operably linked to one another.
Transformation And Cultivation Of Yarrowia lipolvtica
Yarrowia lipolytica strain ATCC #20362 was purchased from the
American Type Culture Collection (Rockville, MD). Yarrowia lipolytica strains
were routinely grown at 28-30 C in several media, according to the recipes
shown below.
High Glucose Media (HGM) (per liter): 80 glucose, 2.58 g KH2PO4 and
5.36 g K2HPO4, pH 7.5 (do not need to adjust).
Fermentation medium (FM) (per liter): 6.70 g/L Yeast nitrogen base,
6.00 g KH2PO4, 2.00 g K2HPO4, 1.50 g MgSO4*7H20, 20 g glucose,
and 5.00 g Yeast extract (BBL).
Transformation of Y. lipolytica was performed as described in U.S. Pat.
Appl. Pub. No. 2009-0093543-A1.
Isolation Of Yarrowia lipolvtica Strain Y4305U
Strain Y4305U, producing EPA relative to the total lipids via expression
of a A9 elongase/A8 desaturase pathway, was generated as described in the
General Methods of U.S. Pat. App. Pub. No. 2008-0254191 .
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Briefly, as diagrammed in FIG. 4, strain
Y4305U was derived from Yarrowia lipolytica ATCC #20362 via construction
of strain Y2224 (a FOA resistant mutant from an autonomous mutation of the
Ura3 gene of wildtype Yarrowia strain ATCC #20362), strain Y4001
(producing 17% EDA with a Leu- phenotype), strain Y4001U1 (Leu- and Ura-
), strain Y4036 (producing 18% DGLA with a Leu- phenotype), strain Y4036U
(Leu- and Ura-), strain Y4070 (producing 12% ARA with a Ura- phenotype),
strain Y4086 (producing 14% EPA), strain Y4086U1 (Ura3-), strain Y4128
(producing 37% EPA; deposited with the American Type Culture Collection
on August 23, 2007, bearing the designation ATCC PTA-8614), strain
Y4128U3 (Ura-), strain Y4217 (producing 42% EPA), strain Y4217U2 (Ura-),
strain Y4259 (producing 46.5% EPA), strain Y4259U2 (Ura-) and strain
Y4305 (producing 53.2% EPA relative to the total TFAs).
The complete lipid profile of strain Y4305 was as follows: 16:0 (2.8%),
16:1 (0.7%), 18:0 (1.3%), 18:1 (4.9%), 18:2 (17.6%), ALA (2.3%), EDA
(3.4%), DGLA (2.0%), ARA (0.6%), ETA (1.7%), and EPA (53.2%). The total
lipid % dry cell weight ["DCW"] was 27.5.
The final genotype of strain Y4305 with respect to wild type Yarrowia
lipolytica ATCC #20362 was SCP2- (YALIOE01298g), YALIOC18711g-,
Pexl 0-, YALIOF24167g-, unknown 1-, unknown 3-, unknown 8-,
GPD::FmD12::Pex20, YAT1::FmD12::OCT, GPM/FBAIN::FmD12S::OCT,
EXP1::FrnD12S::Aco, YAT1::FmD12S::Lip2, YAT1::ME3S::Pex16,
EXP1::ME3S::Pex20 (3 copies), GPAT::EgD9e::Lip2, EXP1::EgD9eS::Lipl ,
FBAINm::EgD9eS::L1p2, FBA::EgD9eS::Pex20, GPD::EgD9eS::Lip2,
YAT1::EgD9eS::Lip2, YAT1::E389D9eS::OCT, FBAINm::EgD8M::Pex20,
FBAIN::EgD8M::Lipl (2 copies), EXP1::EgD8M::Pex16,
GPDIN::EgD8M::Lip1, YAT1::EgD8M::Aco, FBAIN::EgD5::Aco,
EXP1::EgD5S::Pex20, YAT1::EgD5S::Aco, EXP1::EgD5S::ACO,
YAT1::RD5S::OCT, YAT1::PaD17S::Lipl , EXP1 ::PaD17::Pex16,
FBAINm::PaD17::Aco, YAT1::YICPT1::ACO, GPD::YICPT1::ACO (wherein
FmD12 is a Fusarium monitiforme Al2 desaturase gene [U.S. Pat. No.
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7,504,259]; FmD12S is a codon-optimized Al2 desaturase gene, derived
from Fusarium moniliforme [U.S. Pat. No. 7,504,259]; ME3S is a codon-
optimized 016/18 elongase gene, derived from Mortierella alpina [U.S. Pat. No.
7,470,532]; EgD9e is a Euglena gracilis A9 elongase gene [Intl App. Pub.
No. WO 2007/061742]; EgD9eS is a codon-optimized A9 elongase gene,
derived from Euglena gracilis [Intl App. Pub. No. WO 2007/061742];
E389D9eS is a codon-optimized A9 elongase gene, derived from Eutreptiella
sp. CCMP389 [Inn App. Pub. No. WO 2007/061742]; EgD8M is a synthetic
mutant A8 desaturase [Inn App. Pub. No. WO 2008/073271], derived from
Euglena gracilis [U.S. Pat. No. 7,256,033]; EgD5 is a Euglena gracilis A5
desaturase [U.S. Pat. App. Pub. No. 2007-0292924]; EgD5S is a codon-
optimized A5 desaturase gene, derived from Euglena gracilis [U.S. Pat. App.
Pub. No. 2007-0292924]; RD5S is a codon-optimized A5 desaturase, derived
from Peridinium sp. CCMP626 [U.S. Pat. App. Pub. No. 2007-0271632];
PaD17 is a Pythium aphanidermatum A17 desaturase [U.S. Pat. No.
7,556,949]; PaD17S is a codon-optimized A17 desaturase, derived from
Pythium aphanidermatum [U.S. Pat. No. 7,556,949]; and, YICPT1 is a
Yarrowia lipolytica diacylglycerol cholinephosphotransferase gene [Intl App.
Pub. No. WO 2006/052870]).
The Ura3 gene was subsequently disrupted in strain Y4305 (as
described in the General Methods of U.S. Pat. App. Pub. No. 2008-0254191),
such that a Ura3 mutant gene was integrated into the Ura3 gene of strain
Y4305. Following selection of the transformants and analysis of the FAMEs,
transformants #1, #6 and #7 were determined to produce 37.6%, 37.3% and
36.5% EPA of total lipids when grown on MM + 5-FOA plates. These three
strains were designated as strains Y4305U1, Y4305U2 and Y4305U3,
respectively, and are collectively identified as strain Y4305U.
Fatty Acid Analysis Of Yarrowia lipolytica
For fatty acid analysis, cells were collected by centrifugation and lipids
were extracted as described in Bligh, E. G. & Dyer, W. J. (Can. J. Biochem.
Physiol., 37:911-917 (1959)). Fatty acid methyl esters ["FAMEs"] were
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prepared by transesterification of the lipid extract with sodium methoxide
(Roughan, G., and Nishida I., Arch Biochem Biophys., 276(1):38-46 (1990))
and subsequently analyzed with a Hewlett-Packard 6890 GC fitted with a 30-
m X 0.25 mm (i.d.) HP-INNOWAX (Hewlett-Packard) column. The oven
temperature was from 170 C (25 min hold) to 185 C at 3.5 C/min.
For direct base transesterification, Yarrowia culture (3 mL) was
harvested, washed once in distilled water, and dried under vacuum in a
Speed-Vac for 5-10 min. Sodium methoxide (100 ill of 1 %) was added to the
sample, and then the sample was vortexed and rocked for 20 min. After
adding 3 drops of 1 M NaCI and 400 ill hexane, the sample was vortexed and
spun. The upper layer was removed and analyzed by GC as described
above.
EXAMPLE 1
Identification Of Publicly Available Genes Encoding Malonyl-CoA Synthetase
A gene cluster was identified to encode malonyl-CoA decarboxylase
(MatA), malonyl-CoA synthetase (MatB) and a putative dicarboxylate carrier
protein (MatC) in Rhizobium trifolii (An, J.H, & Y. S. Kim, Eur.J. Biochem.,
257:395-402 (1998)).
Using the protein sequence encoding the Rhizobium trifolii malonyl-
CoA synthetase (GenBank Accession No. AF117694 and No. AAC83455;
SEQ ID NO:5), National Center for Biotechnology Information ["NCB11
BLASTP 2.2.19 (Basic Local Alignment Search Tool; Altschul, S. F., et al.,
Nucleic Acids Res., 25:3389-3402 (1997); Altschul, S. F., et al., FEBS J.,
272:5101-5109 (2005)) searches were conducted to identify sequences
having similarity within the BLAST "nr" database (comprising all non-
redundant GenBank CDS translations, the Protein Data Bank ["PDB"] protein
sequence database, the SWISS-PROT protein sequence database, the
Protein Information Resource ["PIR"] protein sequence database and the
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Protein Research Foundation ["PRF"] protein sequence database, excluding
environmental samples from whole genome shotgun ["WGS"] projects).
The results of the BLASTP comparison summarizing the sequence to
which SEQ ID NO:5 has the most similarity are reported according to the %
identity, (:)/0 similarity and Expectation value. "(:)/0 Identity" is defined
as the
percentage of amino acids that are identical between the two proteins. "(:)/0
Similarity" is defined as the percentage of amino acids that are identical or
conserved between the two proteins. "Expectation value" estimates the
statistical significance of the match, specifying the number of matches, with
a
given score, that are expected in a search of a database of this size
absolutely by chance.
A large number of proteins were identified as sharing significant
similarity to the Rhizobium trifolii malonyl-CoA synthetase (GenBank
Accession No. AAC83455; SEQ ID NO:5). Table 3 provides a partial
summary of those hits having an Expectation value equal to "0.0" and
annotation that specifically identified the protein as a "malonyl-CoA
synthetase", although this should not be considered as limiting to the
disclosure herein. The proteins in Table 3 shared between 64% to 94%
identity with SEQ ID NO:5.
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Table 3: Some Publicly Available Genes Encoding Malonyl-CoA Synthetase
GenBank Organism SEQ ID NO
Accession No.
YP_766603
Rhizobium leguminosarum bv. viciae SEQ ID NO:2
3841
YP_468459 Rhizobium etli CFN 42 SEQ ID NO:8
YP_001313848 Sinorhizobium medicae WSM419 SEQ ID NO:9
YP_674146 Mesorhizobium sp. BNC1 SEQ ID NO:10
NP_105559 Mesorhizobium loti MAFF303099 SEQ ID NO:11
YP_001236428 Bradyrhizobium sp. BTAi1 SEQ ID NO:12
YP 779412 Rhodopseudomonas palustris BisA53 SEQ ID NO:13
YP_001526214 Azorhizobium caulinodans ORS 571 SEQ ID NO:14
YP_567622 Rhodopseudomonas palustris BisB5 SEQ ID NO:15
YP_001202443 Bradyrhizobium sp. 0R5278 SEQ ID NO:16
YP_001415433 Xanthobacter autotrophicus Py2 SEQ ID NO:17
YP_483951 Rhodopseudomonas palustris HaA2 SEQ ID NO:18
YP_002210100 Oligotropha carboxidovorans 0M5 SEQ ID NO:19
NP_945574 Rhodopseudomonas palustris CGA009 SEQ ID NO:20
NP_767149 Bradyrhizobium japonicum USDA 110 SEQ ID NO:21
ZP_00629462 Paracoccus denitrificans PD1222 SEQ ID NO:22
,EXAMPLE 2
Synthesis Of A Codon-Optimized Malonyl-CoA Synthetase Gene Of
Rhizobium lequminosarum bv. viciae 3841 For Yarrowia lipolytica
The codon usage of the malonyl-CoA synthetase gene of Rhizobium
leguminosarum bv. viciae 3841 was optimized for expression in Yarrowia
lipolytica, in a manner similar to that described in U.S. Pat. No. 7,125,672.
Specifically, a codon-optimized malonyl-CoA synthetase gene
(designated "MCS", SEQ ID NO:3) was designed based on the coding
sequence of the malonyl-CoA synthetase gene from Rhizobium
leguminosarum bv. viciae 3841 ("rMCS"; SEQ ID NOs:1 and 2, corresponding
to GenBank Accession No. YP 766603) according to the Yarrowia codon
usage pattern (U.S. Pat. No. 7,125,672), the consensus sequence around the
`ATG' translation initiation codon, and the general rules of RNA stability
(Guhaniyogi, G. and J. Brewer, Gene, 265(1-2):11-23 (2001)). In addition to
modification of the translation initiation site, 233 bp of the 1515 bp coding
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region (including the stop codon) were modified (15.4%; FIG. 1) and 219
codons were optimized (43.4%). The GC content was reduced from 61.4%
within the wild type gene (i.e., rMCS) to 55.6% within the synthetic gene
(i.e.,
MCS). The translation initiation codon `ATG' was added in front of the rMCS
gene (SEQ ID NO:1) since Yarrowia cannot use the `GTG' codon for
translation initiation. A Ncol site and Notl sites were incorporated around
the
translation initiation codon and after the stop codon of MCS, respectively.
The codon-optimized MCS gene (SEQ ID NO:3) is 1518 bp encoding a
peptide of 505 amino acids and a stop codon (SEQ ID NO:4). The designed
MCS gene was synthesized by GenScript Corporation (Piscataway, NJ) and
cloned into pUC57 (GenBank Accession No. Y14837) to generate pMCS
(SEQ ID NO:6).
EXAMPLE 3
Generation Of Construct pZP2-MCS, Comprising The Synthetic Malonyl-CoA
Synthetase
Plasmid pZP2-MCS (FIG. 2) was constructed to enable expression of
the synthetic, codon-optimized malonyl-CoA synthetase gene derived from
Rhizobium leguminosarum bv. viciae 3841 (Example 2) in the oleaginous
yeast, Yarrowia lipolytica. The pZP2-MCS plasmid contained the following
components listed in Table 4.
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Table 4: Description of Plasmid pZP2-MCS (SEQ ID NO:7)
RE Sites And Description Of Fragment And Chimeric Gene Components
Nucleotides
Within SEQ ID
NO:7
BsiWII Ascl 803 bp 5' portion of Yarrowia Pox2 gene (GenBank Accession
(318-1128) No. AJ001300)
Sphl/ Pacl 649 bp 3' portion of Yarrowia Pox2 gene (GenBank Accession
(3836-4491) No. AJ001300)
Swal/E3s1W1 FBAIN::MCS::Pex20, comprising:
(6713-318) = FBAIN: Yarrowia lipolytica FBAIN promoter (U.S. Pat.
7,202,356);
= MCS: codon-optimized malonyl-CoA synthetase (SEQ ID
NO:3), derived from Rhizobium leguminosarum bv. viciae 3841
(GenBank Accession No. YP_766603; SEQ ID NO:1);
= Pex20: Pex20 terminator sequence from Yarrowia Pex20 gene
(GenBank Accession No. AF054613)
(4494-5981) Ura3: Yarrowia Ura3 gene (GenBank Accession No. AJ306421)
EXAMPLE 4
Effect Of Malonyl-CoA Synthetase Gene Expression On Malonates In
Yarrowia lipolytica Strain Y4305U
Plasmid pZP2-MCS was digested with Sphl and Ascl. A 6.4 kB linear
fragment containing the MCS gene under the control of the FBAIN promoter
and the Y. lipolytica URA3 gene, flanked by the 5' and 3' region of the Y.
lipolytica PDX2 gene, was separated by agarose gel electrophoresis and
purified with a Qiagen gel purification kit according to the manufacturer's
protocol. The purified DNA fragment was used to transform the Ura3- strain
of Y4305, Y4305U (General Methods), using standard transformation
procedures.
Three Ura+ transformants were tested for lipid content, fatty acid
profile and malonate production; strain Y4305 was also analyzed similarly as
a control. Briefly, cells were grown for 48 hrs in 25 mL of FM medium in a
125 mL flask. Each culture (5 mL) was centrifuged to collect cells. Cells from
each culture were resuspended in 25 mL HGM medium and allowed to grow
for 5 more days at 30 C and 250 rpm. Fatty acid profile and total lipid
content were determined as described in the General Methods.
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To analyze the concentration of malonates in the culture supernatant
by ion chromatography, samples were prepared as follows. 1 mL of a culture
medium sample was centrifuged at 13,000 rpm for 10 min. Supernatant was
collected. Supernatant (0.5 mL) was then put into a PALL nanosep MF 0.2
i.tm (PALL Corporation, East Hills, NY; Cat. No. P/N 0DM02C35) spin tube
and the tube was placed in a microfuge and spun at 13,000 rpm for 15 min.
The filtrate was then diluted with nano-pure water to achieve a concentration
between 0.001 g/L to 0.250 g/L. The analytical vials used for the analysis
were Agilent Technologies (Palo Alto, CA) screw cap vials (Cat. No. P/N
5182-0715).
Concentration of malonates was determined by ion chromatography
with a Dionex DX600 System and a ThermoFinnigan MSQ Mass
Spectrometer. System details, provided by Dionex Corporation (Sunnyvale,
CA), are as follows: lonPac AG11-HC 2 x 50 mm Guard Column, Cat. No.
P/N 052963; lonPac AS11-HC 2 x 250 mm Analytical Column, Cat. No. P/N
052961; ASRS Ultra-II 2 mm Self-Regenerating Suppressor, Cat. No. P/N
061562; Chromeleon Control software, version 6.80. The method used two
detectors in series for both conductivity and mass analysis of the compounds
of interest. A gradient concentration of mobile phase, i.e., KOH, was applied
over the total run time to separate a variety of organic acids. The gradient
was typically 0.5 mM to 60 mM KOH over 64 min to achieve good peak
separation and resolution for all the organic acids and inorganic anions. The
conductivity detector quantitatively determined the compound based on a
standard calibration curve developed from external standards. The mass
spec was used in both the Total Ion Current ["TIC"] and Selective Ion
Monitoring ["SIM"] modes for detecting and identifying each compound and in
some cases for quantifying compounds that co-eluted and that could not be
resolved by conductivity.
Malonates elute at 28.49 min. Quantitation was done by comparing
peak area with that of known amounts of malonate standard (Fluka, Aigma-
Aldrich, Switzerland).
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Total lipid (TFAs (:)/0 DCW), EPA as a (:)/0 of TFAs, and EPA as a (:)/0 of
DCW for each strain are shown below in Table 5, in addition to the
concentration of malonates in each culture. The average fatty acid
composition and average malonate concentration of Y. lipolytica Y4305
control strains and Y4305U strains expressing the codon-optimized malonyl-
CoA synthetase are highlighted in bold text.
More specifically, the term "total fatty acids" ["TFAs"] herein refer to the
sum of all cellular fatty acids that can be derivitized to fatty acid methyl
esters
["FAMEs"] by the base transesterification method (as known in the art) in a
given sample, which may be the biomass or oil, for example. Thus, total fatty
acids include fatty acids from neutral lipid fractions (including
diacylglycerols,
monoacylglycerols and TAGs) and from polar lipid fractions (including the
phosphatidylcholine and phosphatidylethanolamine fractions) but not free
fatty acids.
The term "total lipid content" of cells is a measure of TFAs as a percent
of the dry cell weight ["DCW"], although total lipid content can be
approximated as a measure of FAMEs as a percent of the DCW ["FAMEs (:)/0
DCW"]. Thus, total lipid content ["TFAs (:)/0 DOW"] is equivalent to, e.g.,
milligrams of total fatty acids per 100 milligrams of DCW.
The concentration of a fatty acid in the total lipid is expressed herein
as a weight percent of TFAs ["(:)/0 TFAs"], e.g., milligrams of the given
fatty
acid per 100 milligrams of TFAs. Unless otherwise specifically stated in the
disclosure herein, reference to the percent of a given fatty acid with respect
to
total lipids is equivalent to concentration of the fatty acid as (:)/0 TFAs
(e.g., (:)/0
EPA of total lipids is equivalent to EPA (:)/0 TFAs).
In some cases, it is useful to express the content of a given fatty
acid(s) in a cell as its weight percent of the dry cell weight ["(:)/0 DCW"].
Thus,
for example, eicosapentaenoic acid (:)/0 DCW would be determined according
to the following formula: [(eicosapentaenoic acid (:)/0 TFAs) * (TFAs (:)/0
DCW)]/100. The content of a given fatty acid(s) in a cell as its weight
percent
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of the dry cell weight ["(:)/0 DOW"] can be approximated, however, as:
[(eicosapentaenoic acid (:)/0 TFAs) * (FAMES (:)/0 DCW)]/100.
Table 5: Concentration Of Malonates In Transformant Yarrowia lipolytica
Strain Y4305U
T F As % EPA EPA Malonate (g/g
Sample
DCW (% TFAs) (% DCW) DCW)
Y4305-A 36.8 49.8 18.3 0.462
Y4305-B 35.3 48.8 17.2 0.434
Y4305 Average 36.05 49.3 17.75 0.448
Y4305U-MCS-1 35.2 50.7 17.9 0.029
Y4305U-MCS-2 34.5 49.2 17.0 0.025
Y4305U-MCS-3 36.2 49.5 17.9 0.026
4305U-MCS 35.3 49.8 17.6 0.027
Average
As shown in Table 5, the pZP2-MCS transformants (identified as
Y4305U-MCS-1, Y4305U-MCS-2 and Y4305U-MCS-3) all showed markedly
lower levels of malonates in the culture supernatant, as compared to the level
of malonates in the duplicate cultures of strain Y4305. The profile of fatty
acids and the yield of total lipids are similar to the control Y4305 cells.
Expression of the malonyl-CoA synthetase, i.e., SEQ ID NO:3, lowered the
total amount of malonates (g/g DCW) ¨94% without impacting either the fatty
acid profile or the total lipid yield as a (:)/0 DCW.
67
